Oemedic International, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Oemedic International, Inc. makes
Oemedic International, Inc. manufactures single-use manual resuscitators designed for adult, child, and infant resuscitation. These devices include silicone and standard models, both equipped with masks and reservoir bags for delivering positive-pressure ventilation during emergency care.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Oemedic International Inc. Besmed Single Use Adult, Child, Infant Manual Resuscitator With Mask & Reservoir Ref K021442
Regimes: 510(k) Registry: 510(k)Oemedic International Inc. Besmed Silicone Adult, Child, Infant Manual Resuscitator With Mask And Reservoir Ref K021446
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oemedic International, Inc. have in the registry?
The registry currently lists 2 devices for Oemedic International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oemedic International, Inc.'s devices?
Among its 2 most recently registered devices, Oemedic International, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Oemedic International, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Oemedic International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oemedic International, Inc. in the registry?
The most recently registered devices listed for Oemedic International, Inc. include OEMEDIC INTERNATIONAL INC. BESMED SINGLE USE ADULT, CHILD, INFANT MANUAL RESUSCITATOR WITH MASK & RESERVOIR and OEMEDIC INTERNATIONAL INC. BESMED SILICONE ADULT, CHILD, INFANT MANUAL RESUSCITATOR WITH MASK AND RESERVOIR.