Medi-Dose, Inc.
United StatesFDA applicant, unverified FDA FEI 2521373
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Disposable Disc Filter Ref K936015
Regimes: 510(k) Registry: 510(k)Chemo-Spike Ii Reconstitution Device Ref K974431
Regimes: 510(k) Registry: 510(k)2 Micron Air Eliminating Filter Ref K942532
Regimes: 510(k) Registry: 510(k)Safe Cap Needle Recapping/Uncapping Device Ref K952518
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2521373
- Address
- 70 INDUSTRIAL DRIVE, Warminster, PA, 18974
Frequently asked questions
How many devices does Medi-Dose, Inc. have in the registry?
The registry currently lists 4 devices for Medi-Dose, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi-Dose, Inc.'s devices?
Among its 4 most recently registered devices, Medi-Dose, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Medi-Dose, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medi-Dose, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medi-Dose, Inc. in the registry?
The most recently registered devices listed for Medi-Dose, Inc. include DISPOSABLE DISC FILTER, CHEMO-SPIKE II RECONSTITUTION DEVICE, 2 MICRON AIR ELIMINATING FILTER and SAFE CAP NEEDLE RECAPPING/UNCAPPING DEVICE.