91
000000Ć1150Ć839 IOLMaster 11.02.2004
Medical Product Act
The device meets the requirements of the EC Medical Device Directive
93/42/EEC and of their national equivalent in form of the German
Medical Product Act (MPA).
Device Class as per MPA: IIa
UMDNSĆNo.: 18Ć014
0297
Manufacturer's Declaration
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