Zimmer Patient Care Division
Country not established
- Devices
- 3
What Zimmer Patient Care Division makes
The company manufactures medical devices including an autotransfusion system for blood recovery during surgery, a range of patient restraint vests for hospital use, and general surgery probes with distal perforations for surgical procedures.
These devices are classified under FDA regulations as Class I and Class II, with some models requiring 510(k) clearance. The company’s products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Hemovac Autotransfusion System Ref K920273
510(k) 510(k)- 510(k) 510(k)
- 510(k) 510(k)
Frequently asked questions
How many devices does Zimmer Patient Care Division have in the registry?
The registry currently lists 3 devices for Zimmer Patient Care Division. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zimmer Patient Care Division's devices?
Among its 3 most recently registered devices, Zimmer Patient Care Division has devices listed in FDA 510(k) (3 devices).
What risk classes do Zimmer Patient Care Division's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Zimmer Patient Care Division's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zimmer Patient Care Division in the registry?
The most recently registered devices listed for Zimmer Patient Care Division include HEMOVAC AUTOTRANSFUSION SYSTEM, ECONOMY SAFETY VEST RESTRAINT, SHOULDER TIE SAFETY VEST/SAFETY VEST RESTRAINT, HEAVY DUTY VEST RESTRAINT, MESH SAFETY VE and GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS.