FDA Device Entity Profile: VITROMED GmbH

Known Identifiers & Locations

FEI Numbers 3016126174, 3016214552, 3042228693

Owner Operator Numbers 10062050

Locations Covered Ilion Attiki, GR; Jena Thuringia, DE; Langenfeld (Rheinland) North Rhine-Westphalia, DE

Registered Establishments (3)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
3016126174	VITROMED GmbH	Langenfeld (Rheinland) North Rhine-Westphalia, DE	Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Complaint File Establishment per 21 CFR 820.198	View Details
3016214552	VITROMED GMBH	Jena Thuringia, DE	Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198	View Details
3042228693	VITROMED SMPC	Ilion Attiki, GR	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details

510(k) Premarket Notifications (0)

No 510(k) notifications found for this entity.

FDA Recall History (0)

No recall records found for this entity.

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