CE mark
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The device bears the CE mark
0123
according to the EC directive on medical devices 93/42/EEC and meets the
essential requirements of appendix I of this directive.
The device is classified in class IIa according to appendix IX of the directive.
Manufacturer
Zimmer MedizinSysteme GmbH
Junkersstraße 9
89231 Neu-Ulm, Germany