Omrix Biopharmaceuticals, Ltd.
Country not established
- Devices
- 3
What Omrix Biopharmaceuticals, Ltd. makes
Omrix Biopharmaceuticals, Ltd. makes the EVICEL Application Device, a medical device used for the application of fibrin sealant in surgical settings.
The EVICEL Application Device is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Evicel Application Device Ref K090162
Regimes: 510(k) Registry: 510(k)Crosseal Application Device Ref K030032
Regimes: 510(k) Registry: 510(k)Evicel Application Device Ref K070575
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omrix Biopharmaceuticals, Ltd. have in the registry?
The registry currently lists 3 devices for Omrix Biopharmaceuticals, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omrix Biopharmaceuticals, Ltd.'s devices?
Among its 3 most recently registered devices, Omrix Biopharmaceuticals, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Omrix Biopharmaceuticals, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Omrix Biopharmaceuticals, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omrix Biopharmaceuticals, Ltd. in the registry?
The most recently registered devices listed for Omrix Biopharmaceuticals, Ltd. include EVICEL APPLICATION DEVICE and CROSSEAL APPLICATION DEVICE.