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GB/T 29791.2-2013 Active
GB/T 29791.2-2013 In vitro diagnostic medical devices—Information supplied by the manufacturer (labelling)—Part 2:In vitro diagnostic reagents for professional use
Abstract
This part of GB/T 29791 specifies the requirements for information provided by manufacturers of professional in vitro diagnostic (IVD) reagents.
This part also applies to the information provided by manufacturers of calibrators and control substances intended for use with professional in vitro diagnostic medical devices.
This part also applies to IVD accessories.
This part applies to outer and inner packaging labels and user manuals.
This part does not apply to:
a) in vitro diagnostic instruments or equipment;
b) self-test in vitro diagnostic reagents.
General Product Information
| Document Type | National standards |
|---|---|
| Standard Status | Active |
| Standard Code | GB/T 29791.2-2013 |
| CCS | Medical laboratory equipment |
| ICS | Laboratory medicine |
| Implement Date | 2014-02-01 |
Price
$ 54
Subtotal
$ 54
Tax
$ 0.00
Order Total (incl. tax)
$ 54