This standard was last reviewed* in 2010.
ISO 10993-11:2006 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
Document published on: 2006-08-15 Edition: 2 (Monolingual) ICS: 11.100.20 Status: Published Stage: 90.92 (2015-01-22) TC/SC: ISO/TC 194 Number of Pages: 26
Revised by: ISO/DIS 10993-11
Revises: ISO 10993-11:1993
No corrigenda or amendments available