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SNV - SN EN ISO 18113-2

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use

active, Most Current
Organization: SNV
Publication Date: 1 May 2012
Status: active
Page Count: 24
ICS Code (In vitro diagnostic test systems): 11.100.10
scope:

This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for professional use.

This part of ISO 18113 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for professional use.

This part of ISO 18113 can also be applied to accessories.

This part of ISO 18113 applies to the labels for outer and immediate containers and to the instructions for use.

This part of ISO 18113 does not apply to

a) IVD instruments or equipment,

b) IVD reagents for self-testing.

Document History

SN EN ISO 18113-2
May 1, 2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for professional use. This part of ISO 18113 also applies to information supplied by the...
May 1, 2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for professional use. This part of ISO 18113 also applies to information supplied by the...

References

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