CERTIFICAT CERTIFICATE OF REGISTRATION ISO 13485 : 2016
ISO 13485 : 2016. GMED N° 16553–6. Ce certificat est délivré selon les règles de certification GMED. Début de validité. Valable jusqu'au. / Effective.
ISO 13485:2016
ISO 13485:2016. GUÍA DE IMPLEMENTACIÓN DE SISTEMAS. DE GESTIÓN DE CALIDAD EN PRODUCTOS. SANITARIOS. 50000. GLOBALLY. CERTIFICATES. 90. TRANSPARENT
ISO 13485:2016 Preguntas Frecuentes
¿Los certificados emitidos bajo ISO 13485:2003 o. EN ISO 13485:2012 durante el periodo de transición tendrán una validez limitada? Sí la certificación a ISO
ISO 13485:2016 Preguntas Frecuentes
¿Los certificados emitidos bajo ISO 13485:2003 o. EN ISO 13485:2012 durante el periodo de transición tendrán una validez limitada? Sí la certificación a ISO
NQA ISO13485 Intro Guide.indd
de 2016 anulando las versiones publicadas anteriormente de. 2003 y 1996. La ISO 13485 deriva de la ISO 9001
ISO 13485:2016
Management system as per. Evidence of conformity with the above standard(s) has been furnished. Certificate registration No. 73 105 6685. Audit report No. 4354
ISO 13485:2016 Frequently asked questions
Which version of the Standard should I use for internal audits prior to certification? You will need to ensure that your QMS effectively meets the requirements
Kinova Inc. ISO 13485:2016
Design and manufacturing of sterile nasopharyngeal swab. Certificate Number: 0096652-01. Initial Certification Date: 25 November 2019. Date of Certification
Untitled
14 dic. 2021 ISO 13485:2016 ... The certificate covers the following activities: ... The certificate is valid provided that the quality system continues ...
CERTIFICATE N. CERTIFICADO N. 0462.2020 HEALTHSENS S.L.
Further clarifications regarding the applicability of ISO 13485:2016 requirements may REQUIREMENTS OF THE RULES FOR CERTIFICATION OF MANAGEMENT SYSTEMS.
This is to certify that the management system of:
Kinova Inc.
Main Site: 4333 boul. de la Grande-Allée
Boisbriand, Quebec (Québec), J7H 1M7, Canada
has been registered by Intertek as conforming to the requirements of:ISO 13485:2016
The management system is applicable to:
Design, manufacturing and servicing of robotic arms integrated in medical robotic platforms. Design, manufacturing, installation, and servicing of assistive robotic devices and assistive devices to be used in medical applications. Design and manufacturing of sterile nasopharyngeal swab.Certificate Number:
0096652-01
Initial Certification Date:
25 November 2019
Date of Certification Decision:
26 January 2021
Issuing Date:
26 January 2021
Valid Until:
24 November 2022
In the issuance of this certificate, Intertek assumes no liability to any party other than to the Client, and then only in accordance with the agreed upon Certification Agreement. This
certificate.validation@intertek.com or by scanning the code to the right with a smartphone. The certificate remains the property of Intertek, to whom it must be returned upon
request.CT-ISO 13485_2016-SCC-EN-LT-P-12.dec.17
Calin Moldovean
President
Intertek Testing Services NA Ltd.,
1829, 32nd avenue, Lachine, QC, H8T 3J1,
Canada
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