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BS EN ISO 18113-1:2011

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-Terms, definitions and general requirements

standard by British Standard / European Standard / International Organization for Standardization , 01/31/2012

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Cross References:
ISO 1000
ISO 13485
ISO 14971
ISO 15223-1
IEC 62366
EN 980
ISO 704:2000
ISO 1087-1:2000
ISO 3534-1:2006
ISO 3534-2:2006
ISO 5725-1:1994
ISO 5725-3:1994
ISO 8601
ISO 10241
ISO 15189:2007
ISO 15190:2003
ISO 15193:2002
ISO 15194
ISO 15197:2003
ISO 15198:2004
ISO/IEC 17025
ISO 17511:2003
ISO 17593:2007
ISO 18153
ISO 25680
IEC 60050
IEC 60601-1-6:2006
IEC 61010-2-101:2002
ISO/IEC 80000
ISO/IEC 80416-1:2001
ISO Guide 30:1992
ISO/IEC Guide 51:1999
ISO/IEC Guide 98-3:2008
GUM:1995
ISO/IEC Guide 99:2007
EN 375:2001
EN 376:2002
EN 591:2001
EN 592:2002
EN 13612:2002
EN 13640:2002
CLSI C28-A2:2000
CLSI EP9-A2
CLSI X5-R
CLSI EP12-A2
CLSI EP5-A2
CLSI C51-P
CLSI EP7-A2
CLSI EP17-A
CLSI EP6-A
CLSI GP10-A
ISO 5725-2
ISO 5725-5:1998
ISO 9000:2005
IEC 60050-300:2001
VIM:1993
IEC 60359
98/79/EC


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Product Details

Published:
01/31/2012
ISBN(s):
9780580773273, 9780580769405
Number of Pages:
62
File Size:
1 file , 2.1 MB
Same As:
ISO 18113-1:2009, ISO 18113-1:2009
Product Code(s):
30256217, 30256217
Note:
This product is unavailable in Ukraine, Russia, Belarus
 

Document History

  1. BS EN ISO 18113-1:2011

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    In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-Terms, definitions and general requirements

    • Most Recent

  2. BS EN ISO 18113-1:2009


    In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-Terms, definitions and general requirements

    • Historical Version

  3. BS 06/30146511 DC


    BS ISO 18113-1. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 1. Terms, definitions and general requirements

    • Historical Version