Medical Device Qualified Supplier Directory

 

Dr. Knoell Consult GmbH Company Profile

T: + 49 621 718858-0

Address
Dynamostr. 19, Mannheim, Germany

 

The legal framework for medical devices is determined in the EU by the Medical Devices Directive 93/42/EEC (MDD). This divides medical devices – based on their hazard potential – into four classes (I, II a, II b, III). We advise you with the classification and assist in compiling the technical and regulatory documentation. The classification of your "borderline products" is also in good hands with our specialists

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T: + 49 621 718858-0

Address
Dynamostr. 19, Mannheim, Germany