Greiner Meditech, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Vacuette Holdex Ref K980768
Regimes: 510(k) Registry: 510(k)Vacuette (Multi-Use Holder) Ref K974873
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Greiner Minicollect Edta Blood Collection Tube Ref K982999
Regimes: 510(k) Registry: 510(k)Greiner Vacuette Blood Collection Tube Ref K983952
Regimes: 510(k) Registry: 510(k)Ecomed Scalp Vein Set Ref K992145
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Vacuette Multi-Sample Needle Ref K973620
Regimes: 510(k) Registry: 510(k)Vacuette Multiple Sample Luer Adapter Ref K981619
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Greiner Meditech, Inc. have in the registry?
The registry currently lists 10 devices for Greiner Meditech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Greiner Meditech, Inc.'s devices?
Among its 10 most recently registered devices, Greiner Meditech, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Greiner Meditech, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Greiner Meditech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Greiner Meditech, Inc. in the registry?
The most recently registered devices listed for Greiner Meditech, Inc. include VACUETTE HOLDEX, VACUETTE (MULTI-USE HOLDER), GREINER MINICOLLECT SERUM GEL BLOOD COLLECTION TUBE and GREINER MINICOLLECT EDTA BLOOD COLLECTION TUBE.