Withdrawn
ISO 18113-1:2009 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) medical devices.
NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.
WITHDRAWN
SRPS EN ISO 18113-1:2011
WITHDRAWN
SRPS EN ISO 18113-1:2013
95.99
Withdrawal of Standard
Sep 30, 2024
PUBLISHED
SRPS EN ISO 18113-1:2024