FDA Device Entity Profile: B. BRAUN Avitum AG

Known Identifiers & Locations

FEI Numbers 3002879653, 3004176176, 3004201412, 3007007791, 3007033498, 3014300273

Owner Operator Numbers 9057188

Locations Covered GLANDORF Lower Saxony, DE; MELSUNGEN Hesse, DE; MIRANDOLA Modena, IT; RADEBERG Saxony, DE; Wilsdruff Saxony, DE

Registered Establishments (6)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
3002879653	B. Braun Avitum AG	MELSUNGEN Hesse, DE	Complaint File Establishment per 21 CFR 820.198	View Details
3004176176	B. Braun Avitum AG	GLANDORF Lower Saxony, DE	Export Device to the United States But Perform No Other Operation on Device	View Details
3004201412	B. Braun Avitum Saxonia GmbH	RADEBERG Saxony, DE	Manufacture Medical Device	View Details
3007007791	B. BRAUN AVITUM AG	MELSUNGEN Hesse, DE	Manufacture Medical Device	View Details
3014300273	B.Braun Avitum Saxonia GmbH	Wilsdruff Saxony, DE	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
9681240	B. Braun Avitum Italy S.p.A.	MIRANDOLA Modena, IT	Manufacture Medical Device,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.

Profile Disclaimer

AvaSpecs compiles public data records from the FDA database. This compiled profile does not indicate endorsement, safety, clearance, approval, or compliance status. AvaSpecs is a private search index and is not affiliated with the FDA or any government agency.