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DANSK DSF/FPRCEN/TR 17223 PDF

DANSK DSF/FPRCEN/TR 17223 PDF

Name:
DANSK DSF/FPRCEN/TR 17223 PDF

Published Date:

Status:
[ Draft ]

Description:

Guidance on the relationship between EN ISO 13485: 2016 (Medical devices – Quality management systems – Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation

Publisher:
Dansk Standard

Document status:
Active
Format:
Electronic (PDF)
Delivery time:
10 minutes
Delivery time (for Czech version):
200 business days
SKU:
dansk-dsf-fprcen-tr-17223_2719987
Choose Document Language:
20.70 €
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This Technical Report provides guidance on the relationship between the requirements in the European Regulations for Medical Device and In Vitro Diagnostic Medical Devices and EN ISO 13485:2016 – Medical devices – Quality management systems – Requirements for regulatory purposes.


Edition : 17
File Size : 1 file , 1.3 MB
Number of Pages : 87
Product Code(s) : DSF-061, DSF-061

History

DANSK DSF/FPRCEN/TR 17223
DANSK DSF/FPRCEN/TR 17223
Published Date:
Guidance on the relationship between EN ISO 13485: 2016 (Medical devices – Quality management systems – Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation
20.70 €
DANSK DS/CEN/TR 17223
DANSK DS/CEN/TR 17223
Published Date: 03/27/2018
Guidance on the relationship between EN ISO 13485: 2016 (Medical devices – Quality management systems – Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation
35.70 €

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