Medegen Medical Manufacturing Services, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
- Regimes: 510(k) Registry: 510(k)
Drug Access Spike Ref K051930
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Tru-Swab Stocock Ref K052330
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medegen Medical Manufacturing Services, Inc. have in the registry?
The registry currently lists 5 devices for Medegen Medical Manufacturing Services, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medegen Medical Manufacturing Services, Inc.'s devices?
Among its 5 most recently registered devices, Medegen Medical Manufacturing Services, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Medegen Medical Manufacturing Services, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Medegen Medical Manufacturing Services, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medegen Medical Manufacturing Services, Inc. in the registry?
The most recently registered devices listed for Medegen Medical Manufacturing Services, Inc. include MAXGUARD ADVANCED LUER ACTIVATED DEVICE WITH ANTIMICROBIAL, DRUG ACCESS SPIKE, INTRAVASCULAR ADMINISTRATION SET AND EXTENSION SET and TRU-SWAB STOCOCK.