Hello. Sign In
Standards Store

DS/EN ISO 18113-3

2011 Edition, December 19, 2011

Complete Document

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use



Detail Summary

Active, Most Current

EN
Additional Comments:
SAME AS ISO 18113-3
Format
Details
Price (USD)
PDF
Single User
$69.00
Print
In Stock
$69.00
PDF + Print
In Stock
$110.40 You save 20%
Add to Cart

People Also Bought These:

CSRS LEVEL 3
IEC/TR 62348
J-STD-001
IEC 61010-2-101

Product Details:

  • Revision: 2011 Edition, December 19, 2011
  • Published Date: December 19, 2011
  • Status: Active, Most Current
  • Document Language: English
  • Published By: Dansk Standardiseringsrad (DS)
  • Page Count: 26
  • ANSI Approved: No
  • DoD Adopted: No

Description / Abstract:

ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use. ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD instruments for professional use. ISO 18113-3:2009 can also be applied to accessories, where appropriate.