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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

standard by BSI Group , 12/07/2006

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Cross References:
ISO 1000
ISO 3534-1
ISO 3534-2
ISO 5725-1
ISO 8601
ISO 13485
ISO 14971
IEC 62366
ISO 15223
EN 980
VIM:1993
ISO 1000:1992
ISO 3534-1
ISO 3534-2
ISO 5725-1
ISO 5725-3:1994
ISO 13485
ISO 14971:2000
ISO 15189:2003
ISO 15190:2003
ISO 15193:2002
ISO 15197:2003
ISO 15198:2004
ISO 15223:2000
ISO 17511:2003
ISO DIS 17593
ISO 18153
ISO Guide 30:1992
GUM:1995
ISO/IEC Guide 51:1999
ISO/IEC 17025:2005
ISO/IEC 80416-1:2001
ISO REMCO
IEC 60601-6
IEC 61010-2-101
IEC/CDV 62366:2004
EN 375:2001
EN 376:2002
EN 591:2001
EN 592 :2001
EN 980:2003
EN 13612:2002
EN 13640:2002
VIM:1993
VIM:1994
CLSI C28-A2
CLSI C53-P
CLSI EP5-A2
CLSI EP6-A
CLSI EP7-A2
CLSI EP9-A2
CLSI EP12-A
CLSI EP17-A
CLSI GP10-A
98/79/EC:1998
 

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Published:
12/07/2006
Number of Pages:
40
 

Document History

  1. BS EN ISO 18113-1:2011


    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

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    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