FDA Device Entity Profile: Aesculap AG

Known Identifiers & Locations

FEI Numbers 3001354499, 3002806315, 3008711893

Owner Operator Numbers 8010193

Locations Covered CHAUMONT Grand Est, FR; Suzhou Jiangsu, CN; TUTTLINGEN, DONAU Baden-Wurttemberg, DE

Registered Establishments (3)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
3008711893	B.Braun Medical (Suzhou) Co,.Ltd	Suzhou Jiangsu, CN	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
9610612	AESCULAP AG	TUTTLINGEN, DONAU Baden-Wurttemberg, DE	Manufacture Medical Device	View Details
9681258	AESCULAP SAS	CHAUMONT Grand Est, FR	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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