The CE marking is the only mandatory certificate in order to market a medical device within the European Community. Analyzes and certifications on the material at accredited laboratories, demonstrates the biocompatibility of the medical device.

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DIN-EN-ISO 13485:2003

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Certification

ce

 

(CEE 93/42)

NACERA PEARL AND SHADED
LIQUID COLORS E BLUE-X

Other certifications

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FDA 510(k) USA

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ISO 13485 & ISO 9001 CMDCAS

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Health Canada License

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Mexico Registration

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flagge brasilen

Brazil-Certification

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flagge australien

Australian Register ARTG

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flagge china

China Food & Drug Adminstration

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