FDA Device Entity Profile: Getinge

Known Identifiers & Locations

FEI Numbers 1000125215, 3000231474, 3012068831, 3025504317

Owner Operator Numbers 10055718, 9057664

Locations Covered E Windsor, NJ, US; Englewood, CO, US; Plewiska Wielkopolskie, PL; VAXJO Kronoberg, SE

Registered Establishments (4)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
2028456	STERITEC PRODUCTS MFG. CO., INC.	Englewood, CO, US	Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device	View Details
3012068831	Getinge IC Production Poland sp. z o.o.	Plewiska Wielkopolskie, PL	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
3012092534	Getinge Group Logistics America, LLC	E Windsor, NJ, US	Repack or Relabel Medical Device	View Details
9616031	GETINGE DISINFECTION AB	VAXJO Kronoberg, SE	Manufacture Medical Device	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

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