FEEDING CHAIR FOR CHILDREN

Transcription

1 Page 1 of 15 Prepared by : Diego Alves de Oliveira Verified by : Karen C. Martins Approved by : Maria Lucia Hayashi Approval Date : 02/06/ OBJECTIV Establish the requirements for the conformity assessment Program for Feeding Chairs for children, with a focus on safety in the use of the product, taking into account the quality technical regulation for Feeding Chairs for children, aiming at the prevention of accidents of consumption. On the simplification of reference in the text of this Certification rule complement, any type of feeding chair for children in this document is named "Chair". 1.1 Scope of application This CRC applies to feeding chairs for children of high type, with or without tray, and chairs of fitting in tables Feeding chairs that can be converted into other items, such as low chair, low chair and table, Walker, stand for children, swing, baby comfort, child restraint device, reclining chair for babies, or other, must meet the requirements of the CRC, in addition to meeting the specific regulation for another function, if it exists This CRC does not apply to chairs and portable seats for children who are fixed in common chairs. 1.2 Grouping for the purposes of certification and registration For the certification and registration of the object of this CRC, applies the concept of brand/model The models of feeding chairs for children are as examples that feature the same construction materials, dimensions, load capacity, locking devices and type of support/base anchoring Different colors and prints feature variations of the same model. 2 ACRONYMS ABNT CNPJ CRC IAF INMETRO ISO MLA MPE NBR RAC RC RGCP RTQ SGQ Brazilian Association of technical standards National registry of Legal Person Certification Rule Complement International Accreditation Forum National Institute of metrology, standardization and Industrial quality International Organization for Standardization Multilateral Recognition Arrangements Micro and small enterprise Brazilian Standard Conformity assessment requirements Certification rule General requirements for product Certification Quality technical regulation Quality management system

2 Page 2 of ADDITIONAL DOCUMENTS ABNT NBR : High chairs for children Part 1:Safety requirements; ABNT NBR : High chairs for children Part 2:Test methods; ABNT NBR ISO 9001: Quality management systems Fundamentals and Vocabulary; ORDINANCE INMETRO nº 51, de 01 de Fevereiro de Approving the conformity assessment Requirements for Fedding Chairs for children, or its complement or substitute; ORDINANCE INMETRO n 683, de 21 de Dezembro de Approves the quality technical regulation for Feeding Chairs for children, or its complement or substitute; ORDINANCE INMETRO nº 359, de 01 de Agosto de 2014 Establishes the time limit for demanding corrosion test. ORDINANCE INMETRO nº 118, de 06 de Março de Approves the General requirements for product Certification RGCP, or its complement or substitute; ORDINANCE INMETRO nº 491, de 13 de Dezembro de Approves the procedure for the granting, maintenance and renewal of the object record, or its complement or substitute. 4 - DEFINITIONS For purposes of this CRC, are adopted definitions cited in the RTQ, complemented by the RGCP settings. 5 - CONFORMITY ASSESSMENT MECHANISMS The conformity assessment mechanism for feeding Chair for children is the compulsory certification, to be conducted by TÜV Rheinland of Brazil Ltda, henceforth called TÜV, duly accredited in the scope of this CRC by CGCRE. 6. STEPS OF CONFORMITY ASSESSMENT 6.1 Certificate template definition The certification models used for the products covered by this CRC are described below, and the supplier chooses one of them. Certification model 4 -Type test followed by verification test on samples taken in trade, as described in item 6.3 of this CRC, being valid only for national manufacturers showing their classification as MPE and/or to national craftsmen. Certification model 5 -Type test, evaluation and approval of quality management system of the manufacturer, monitoring through audits in the manufacturer and testing on samples taken in trade, as described in item 6.4 of this CRC; Certification model 7 -Batch test, as described in item 6.5 of this CRC. 6.2 Initial Assessment In this item are described the initial steps of the conformity assessment process, culminating in the attestation of conformity of Chair. Note: The steps to Request certification and examination of the request and the conformity of the documentation described in items and of this CRC, are common to all models of certification. The other conformity assessment steps are specified separately for each model on items 6.3, 6.4 and 6.5 of this CRC Certification request The supplier shall forward a formal request, as form 733-FO-010 to TÜV, which shall include, along with the documentation described in 700 RC-001 the following items:

3 Page 3 of 15 a) Descriptive Memorial, as Annex B of this CRC; b) In the case of certification option for Model 4, the supplier shall demonstrate the TÜV, what criteria of traceability that he uses; c) In the case of certification option for Model 5, documentation of the quality management system in compliance with the requirements described in section or item for the case of MPEs; d) In the case of certification option for Model 7, identification of the lot size to be certified. Note: The MPEs must submit documents proving their classification in accordance with current legislation. Fits the TÜV, evaluate and validate this classification Analysis of the request and the conformity of the documentation The criteria for Analysis of the request and the conformity of the documentation should follow the General guidelines described in RGCP. TÜV, upon receiving the documentation specified, opens a process of granting the certificate of conformity and performs an analysis as to the relevance of the request, as well as an assessment of the conformity of the documentation forwarded by the requestor, If non-compliance is identified in the documentation received, this is formally forwarded to the applicant for its correctness and proper formalization by the TÜV, aiming to highlight the implementation of same (s) for further analysis. Critical analysis will be evidenced in the form 733-FO Certification model 4 - Type test followed by verification test on samples taken in trade The model 4 certification should be used only as an option for national manufacturers showing their classification as MPE and/or to national craftsmen Initial test plan The TÜV shall establish the initial test plan according to the criteria set out in RGCP and this CRC, being evidenced in the form 733-FO-014. The initial test plan should contemplate the sampling is specified in item Definition of Visual inspections, Tests and/or measurements to be made The tests applicable to high chairs are listed in item 6.1 of the RTQ, and the tests applicable to fit chairs in the table are listed in item 6.2 the RTQ. The Visual inspections and/or measurements to be performed are listed in items 5.1.1, 5.2.5, , , , and the RTQ Sampling Definition TÜV is responsible for random collection of samples of the Chair to be certified, which should be identified, sealed and forwarded to the laboratory for testing, as 700 forms-fo-016 and 700-FO For each feeding chair model, TÜV must collect sample (proof, counter-proof and witness) to verify the requirements described in the RTQ. The number of samples and the acceptance criteria for each test, Visual inspection and/or measurements are specified in tables 1 and 2 below. The tests shall be performed in the order in which they appear in the tables.

4 Page 4 of 15 Table 1: Sampling for testing, Visual inspections and/or measurements for high chairs Sampling Visual inspections, tests and/or measurements Counterproof Proof Witness Acceptance criteria Visual inspection of materials According item do RTQ Visual inspection of bolts Visual inspection of the retention device Visual inspection of the locking mechanism Visual inspection of wheels and brakes Migration of chemical elements test Salt fog test Fabric shrinkage test (applicable only for chairs made with fabrics that can be removed for washing) Assembly inspection Testing of edges, corners and protruding parts Impact test Tests of the locking mechanism Testing of wheel locks (applicable only for chairs with wheels or casters) Small parts testing Tests of holes, cracks and openings Moving parts Retention device tests Measurement of the height of the side protection Seat tests Dynamic testing of seat (applicable only for chairs without a rigid base under the seat) Vertical static load test of the seat Vertical static load test of the footrest (applicable only for chairs with footrests, removable or not) Stability tests Tray tests Marking and instructions for use Total sampling by According item do RTQ According itens e do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ According item do RTQ

5 Page 5 of 15 make/model Table 2: Sampling for testing, Visual inspections and/or measurements to fit chairs in table Visual inspections, tests Sampling and/or measurements Proof Contraprova Witness Acceptance criteria Visual inspection of materials According item do RTQ Visual inspection of bolts According item do RTQ Visual inspection of the retention device Accordings itens e do RTQ Visual inspection of the locking mechanism According item do RTQ Visual inspection of wheels and brakes According item do RTQ Visual inspection of the footrest According item do RTQ Migration of chemical elements test According item do RTQ Salt fog test According item do RTQ Flammability test of fabric According item do RTQ Fabric shrinkage test According item do RTQ Assembly inspection According item do RTQ Testing of edges, corners and protruding parts According item do RTQ Tests of holes, cracks and openings According item do RTQ Moving parts According item do RTQ Small parts testing According item do RTQ Tests of the locking According item do RTQ mechanism Seat tests According item do RTQ Support test of anchoring According item do RTQ Retention device tests According item do RTQ Test of stability According item do RTQ Swing test According item do RTQ Measurement of height of side protection According item do RTQ Backrest height measurement According item do RTQ Marking and instructions for use According item do RTQ Total sampling by make/model 2 2 2

6 Page 6 of All tests, visual inspections and/or measurements must be carried out on the proof sample If the results of all tests, Visual inspections and/or measurements conform, the product should be considered approved If you checked any non-compliant result on the test, the sample shall be considered failed.in this case, non-compliance detected in the test shall be recorded by means of the product non-conformity report as form 700-FO-13, and forwarded to the supplier for your due actions In case of disapproval of the sample test, the supplier may choose to correct the non-conformity identified by TÜV. In this case, the process only continues after the supplier present new samples for tasting, and counter-proof witness to repeat all tests, Visual inspections and/or measurements If the supplier chooses to use the counter-proof shall be subjected to the test (s), Visual inspections and/or measurements in which the sample test has failed. If you checked any non-compliant result in counter-proof, the sample and the product must be considered disapproved If the results of the tests, Visual inspections and/or measurements performed in the sample of counter-proof conform, must be repeated in witness sample testing, visual inspections and/or measurements in which the sample test has failed. If you checked any results not as a witness, the sample and the product must be considered disapproved, otherwise approved In case of disapproval of the witness and of the product sample, the supplier may choose to treat the non-conformity, in accordance with item In this case, the supplier should clearly show the effectiveness of corrective action featuring new samples for tasting, and counter-proof witness to repeat all tests, Visual inspections and/or measurements Definition of Laboratory The definition of laboratory must follow the conditions described in the 700-RC Treatment of non-conformities at the initial assessment stage The criteria for treatment of non-conformities in the initial assessment stage must follow the requirements set out in the RGCP Issue of certificate of conformity The criteria for the issuance of the certificate of conformity at the initial assessment stage must follow the conditions described in the 700-RC-001. Still, for the issuance of the certificate, it will require the elaboration of a technical report of the certification process, as form 700-FO-24, in order to highlight the criteria for attendance to the RAC and RTQ and other applicable requirements and present the critical analysis of the procedure for certification of the product in question. Will also be drafted the check list for approval of the certification process, as form 700-FO-001, to verify the completeness and appropriateness of the activity/requested document. Critical analysis for the certificate will be reported on the form 733-FO Certification Commission The criteria for the Certification Commission must follow the requirements set out in the RGCP The analysis made by the Certification Commission shall be performed by sample, and not have the purpose to authorize or validate the Certificates of Conformity, but is useful to indicate improvements in the process.

7 Page 7 of Certificate of conformity The certificate of conformity must have validity of 4 (four) years and contain the following wording: "the validity of this certificate is tied to the performance of evaluations of maintenance and treatment of possible non-conformities according to TÜV guidelines" The certificate of conformity, as a formal instrument issued by TÜV, must contain, in addition to the information referred to in RGCP, at least the following information, which should be issued in the form 700-CE-33: a) Certification model adopted; b) Number and date of test report issued by the laboratory; c) Manufacturing unit of the certified product; d) Requestor's name and address of the certification; e) Scope of certification and license for use of the trademark is granted, including the certified product, sorted by model, type or class of products and product standards with which the product has been certified; f) The effective date of certification, the date of issue of the certificate and validity of certification Registration of the object After the issuance of the certificate of compliance, the provider shall request the registration of the object by the Inmetro, according to ORDINANCE No. 491/Inmetro 2010 or his substitutionary, attaching to the Orchestra System the following document, in addition to those required by this ORDINANCE: a) Contract of business relationship between manufacturer/importer and supplier, where the supplier is not the manufacturer/importer of the object to be registered Maintenance assessment The assessment of maintenance should be scheduled by TÜV, according to the criteria laid down in the subsequent steps Maintenance Testing plan Maintenance tests should be performed and recorded, given the steps described below, as evidenced in the form 733-FO Definition of tests that will be carried out Maintenance tests must be conducted and concluded within 12 (twelve) months in accordance with item this CRC Translate sampling of Maintenance For the carrying out of the tests, TÜV maintenance should carry out purchase or random collection of samples from the certificate templates. Must be in compliance with the conditions described in section this CRC Definition of Laboratory The definition of laboratory should follow must follow the conditions described in the 700-RC Treatment of non-conformities in step Maintenance assessment The criteria for treating non -conformities in the Maintenance Assessment step must follow the requirements set out in RGCP TÜV should issue a corrective action tracking Report detailing the actions taken for the Elimination of non-conformities and the evidence of implementation and its effectiveness.

8 Page 8 of TÜV must attach the test reports provided by the laboratory, when available, to the follow-up report of corrective actions Confirmation of Maintenance The criteria for confirmation of maintenance must follow the requirements set out in the RGCP Recertification evaluation General assessment criteria for recertification are referred to in RGCP. The deadline for recertification is 4 (four) years Treatment of non-conformities in step of Recertification The criteria for treatment of non-conformities in the recertification assessment step must follow the requirements set out in the RGCP Confirmation of Recertification The criteria for confirmation of recertification must follow the requirements set out in the RGCP. 6.4 Certification model 5 - Type test, evaluation and approval of quality management system of the manufacturer, monitoring through audits in the manufacturer and testing on samples taken in market Initial audit of quality management Systems The criteria for the Initial Audit of the management system should follow the General guidelines described in RGCP Addition to the requirements referred to in item of RGCP, TÜV must assess the QMS of the productive process of the Chair in accordance with the requirements of Table 3, using 700 forms-fo-10-b, 733-FO-11. Table 3: Itens to be verified according standard ABNT NBR ISO 9001 REQUIREMENTS OF THE QMS ABNT NBR ISO 9001 Quality manual For MPE, the assessment of the QMS of the productive process of the Chair should be held by OCP based on the scope of the certification process and according to the following Table 4. Table 4: Itens to be verified according standard ABNT NBR ISO 9001 for MPE REQUIREMENTS OF THE QMS ABNT NBR ISO 9001 Control of records Communication with the client Procurement process Verification of purchased product Identification and traceability Preservation of product Customer satisfaction Monitoring and measurement of product Control of non-conforming product 8.3 Corrective action 8.5.2

9 Page 9 of Initial test plan TÜV shall establish the initial tests plan Accordings criteria set out in RGCP and this CRC, being evidenced in the form 733-FO-014. The initial test plan should contemplate the sampling is specified in item Definition of Visual inspections, Tests and/or measurements to be made The tests applicable to high chairs are listed in item 6.1 of the RTQ, and the tests applicable to fit chairs in the table are listed in item 6.2 of RTQ. The Visual inspections and/or measurements to be performed are listed in items 5.1.1, 5.2.5, , , , and of RTQ Sampling Definition The criteria for definition of sampling shall follow the conditions laid down in item this CRC Definition of Laboratory The definition of laboratory must follow the conditions described in the 700-RC Treatment of non-conformities at the initial assessment stage The criteria for treatment of non-conformities in the initial assessment stage must follow the requirements set out in the RGCP Issue of certificate of conformity The criteria for the issuance of the certificate of conformity at the initial assessment stage must follow the conditions described in the 700-RC-001. Still, for the issuance of the certificate, it will require the elaboration of a technical report of the certification process, as form 700-FO-24, in order to highlight the criteria for attendance to the RAC and RTQ and other applicable requirements and present the critical analysis of the procedure for certification of the product in question. Will also be drafted the check list for approval of the certification process, as form 700-FO-001, to verify the completeness and appropriateness of the activity/requested document. Critical analysis for the certificate will be reported on the form 733-FO Certification Commission The criteria for the Certification Commission must follow the requirements set out in the RGCP The analysis made by the Commission for Certification should be held amostralmente and aims not to authorize or validate the certificates of conformity, but rather, serve to indicate improvements in the process Certificate of conformity The certificate of conformity must have validity of 4 (four) years and contain the following wording: "the validity of this certificate is tied to the performance of evaluations of maintenance and treatment of possible non-conformities according to TÜV guidelines" The certificate of conformity, as a formal instrument issued by TÜV, must contain, in addition to the information referred to in RGCP, at least the following information, which should be issued in the form 700-CE-33: a) Certification model adopted; b) Number and date of test report issued by the laboratory; c) Unidade fabril do produto certificado; d) Requestor's name and address of the certification;

10 Page 10 of 15 e)scope of certification and license for use of the trademark is granted, including the certified product, sorted by model, type or class of products and product standards with which the product has been certified; f) The effective date of certification, the date of issue of the certificate and validity of the certification Registration of the object After the issuance of the certificate of compliance, the provider shall request the registration of the object by the Inmetro, according to ORDINANCE No. 491/Inmetro 2010 or their substitution by attaching to the system the following document, in addition to those required by the said ORDINANCE: a) contract of business relationship between manufacturer/importer and supplier, where the supplier is not the manufacturer/importer of the object to be registered Maintenance assessment The assessment of maintenance should be scheduled by TÜV, according to the criteria laid down in the subsequent steps Maintenance audit The maintenance audit criteria are referred to in RGCP. The audit should be conducted and completed every 12 (twelve) months The TÜV must assess the QMS in accordance with the manufacturer's item of this CRC Maintenance Testing plan These tests shall be performed and recorded, given the steps described below, as evidenced in the form 733-FO Definition of tests that will be carried out Maintenance tests must be conducted and concluded within 12 (twelve) months in accordance with item this CRC Maintenance Sampling Definition For the carrying out of the tests, TÜV maintenance should carry out purchase or random collection of samples. Must be in compliance with the conditions described in section this CRC Definição do Laboratório The definition of laboratory must follow the conditions described in the 700-RC Treatment of non-conformities in step Maintenance assessment The criteria for treatment of non-conformities in step maintenance assessment should follow the requirements laid down in RGCP TÜV should issue a corrective action tracking Report detailing the actions for elimination of nonconformities and the evidence of implementation and its effectiveness TÜV must attach the test reports provided by the laboratory, when available, to the follow-up report of corrective actions Confirmation of Maintenance The criteria for confirmation of maintenance must follow the requirements set out in the RGCP.

11 Page 11 of Recertification evaluation General assessment criteria for recertification must follow the requirements set out in RGCP. The deadline for recertification is 4 (four) years Treatment of non-conformities in step of Recertification Treatment of non-conformities in step of Recertification Confirmation of Recertification The criteria for confirmation of recertification must follow the requirements set out in the RGCP. 6.5 Certification model 7 - Batch test Test plan TÜV shall establish the initial tests plan Accordings requirements laid down in RGCP and this CRC, being evidenced in the form 733-FO-014. The initial test plan should contemplate the sampling is specified in item Definition of the tests, Visual inspections and/or measurements to be made The tests applicable to high chairs are listed in item 6.1 of the RTQ, and the tests applicable to fit chairs in the table are listed in item 6.2 of RTQ. The Visual inspections and/or measurements to be performed are listed in items 5.1.1, 5.2.5, , , , and of RTQ Sampling Definition TÜV is responsible for random collection of samples of the Chair to be certified, by brand/model, as shown in the following Table 5. Tests As Tables 1 and 2 of this CRC Table 5: Sampling for testing for certification of models of chairs Sampling Lot size Proof Counter-proof Witness 1 a a a Equal or above de Table 5 sampling should be divided proportionately to the tests, Visual inspections and/or measurements established by Tables 1 and 2 of this CRC The sample must be identified, sealed and sent to the lab, according to the established in specific procedure of TÜV as 700 forms-fo-016 and 700-FO All testes, Visual inspections and/or measurements must be carried out on the proof sample. If the results of all tests, Visual inspections and/or measurements conform, the product shall be considered approved. If you checked any non-compliant result on the test, the sample shall be considered failed In case of disapproval of the proof sample, the supplier may choose to use the counter-proof, subjecting to the test (s), Visual inspections and/or measurements in which the sample test has failed. If you checked any non-compliant result in counter-proof, the sample and the product must be considered disapproved.

12 Page 12 of If the results of the tests, Visual inspections and/or measurements performed in the sample of counter-proof conform, must be repeated in witness sample testing, Visual inspections and/or measurements in which the sample test has failed. If you checked any results not as a witness, the sample and the product must be considered disapproved, otherwise approved Definition of Laboratory The definition of laboratory must follow the conditions described in the 700-RC Treatment of non-conformities In case of disapproval of the lot, the product cannot be released for marketing in the domestic market Issue of certificate of conformity The criteria for issue of the certificate of conformity must follow the requirements set out in the RGCP Certification Commission The criteria for the Certification Commission must follow the requirements set out in the RGCP Certificate of conformity The certificate of compliance has its validity indefinite, being valid only for the lot in question, which should be mentioned in the certificate. Still, for the issuance of the certificate, it will require the elaboration of a technical report of the certification process, as form 700-FO-24, in order to highlight the criteria for attendance to the RAC and RTQ and other applicable requirements and present the critical analysis of the procedure for certification of the product in question. Will also be drafted the check list for approval of the certification process, as form 700-FO-001, to verify the completeness and appropriateness of the activity/requested document. Critical analysis for the certificate will be reported on the form 733-FO The certificate of conformity, as a formal instrument issued by TÜV, must contain, in addition to the information referred to in RGCP, at least the following information, which should be issued in the form 700- CE-33: a) Certification model adopted; b) Identification of the batch (number of LI, serial number of the products that make up the batch, quantity, date of manufacture), where applicable; c) Number and date of test report issued by the laboratory; d) Manufacturing unit of the product certificate; e) Requestor's name and address of the certification; f) The effective date of certification and the date of issue of the certificate Registration of the object After the issuance of the certificate of compliance, the provider shall request the registration of the object by the Inmetro, according to ORDINANCE No. 491/Inmetro 2010 or his substitutionary, attaching to the Orchestra System the following document, in addition to those required by this ORDINANCE: a) Contract of business relationship between manufacturer/importer and supplier, where the supplier is not the manufacturer/importer of the object to be registered. 7 TREATMENT OF COMPLAINTS Criteria for processing of claims must follow the conditions described in the 700-RC-001.

13 Page 13 of 15 8 ACTIVITIES PERFORMED By FOREIGN OAC The criteria for activities performed by foreigners OAC must follow the requirements set out in the RGCP. 9 TERMINATION OF CERTIFICATION The criteria for termination of Certification must follow the requirements set out in the RGCP. 10 IDENTIFICATION SEAL OF COMPLIANCE The general criteria for the identification of conformity Seal should follow the requirements laid down in RGCP and in Annex A of this CRC. 11 AUTHORIZATION FOR USE OF THE SEAL OF IDENTIFICATION OF CONFORMITY The criteria for authorization to use the seal of Identification of compliance must follow the conditions described in the 700-RC-001 and the current Object registration ORDINANCE. 12 RESPONSIBILITIES AND OBLIGATIONS The criteria for responsibilities and obligations must follow the conditions described in the 700-RC MARKET MONITORING 14 PENALTIES The criteria for monitoring should follow the requirements laid down in RGCP. The criteria for application of penalties must follow the conditions described in the 700-RC COMPLAINTS The TÜV Rheinland of Brazil offers the following channels for complaints, complaints and suggestions: qualidade@br.tuv.com Site: tuvbrasil.com.br Phone: (+5511) Inmetro offers the following channels of the Ombudsman for complaints, complaints and suggestions: ouvidoria@inmetro.gov.br; Phone : (+55) ; Sítio: 16 CHANGES MADE Data Issue Responsible 20/03/2013 Inicial Robynson Molinari 01/09/2014 Inclusion of forms Diego Alves de Oliveira 06/01/2015 Changing the encoding of the document Ana Paula Tamasia 02/06/2015 Amendment of the codification of the forms, and date of the regulation Diego Alves de Oliveira

14 Page 14 of 15 ANNEX A MODELS FOR THE IDENTIFICATION OF CONFORMITY SEAL A.1The identification of conformity Seal must be affixed to the product and the packaging clearly indelibly and inviolable, in visible location, printed (in the form of adhesive or not), and may follow one of the models described in figure a. 1. Figure A.1 Shapes and dimensions of Compliance Identification Label.

15 Page 15 of 15 ANNEX B - DESCRIPTIVE MEMORIAL B.1 Should be drawn up for each type of descriptive memorial Chair, which should contain at least the information below: 1 - GENERAL DATA BUSINESS NAME OF THE MANUFACTURER/IMPORTER: ADDRESS OF THE MANUFACTURER/IMPORTER NAME of the MANUFACTURER/importer (if applicable): MODELS OF CHAIRS: BUSINESS NAMES: 2 - GENERAL CHARACTERISTICS OF THE CHAIR MATERIAL: MANUFACTURING PROCESS: DIMENSIONS: TYPE OF CHAIR: ( ) HIGH CHAIR ( ) TABLE CHAIR LOAD CAPACITY: ACCESSORIES 3 - POSITIONING OF THE MANDATORY MARKINGS (SEAL) MAKER'S MARK and or importer: Indicate the product positioning. SEAL of COMPLIANCE IDENTIFICATION: Indicate the product positioning. 4 - ATTACHMENTS Attach drawings and/or Technical Catalogues. Date of the document Signatures of the responsible of the supplier Reviewed by TÜV Rheinland in: / /