Beech Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Beech Medical, Inc. makes
Beech Medical, Inc. manufactures infusion pumps and intravenous (IV) administration sets, including extension sets, retrograde administration sets, and mini-volume IV sets designed for controlled fluid delivery in clinical settings.
The company’s products are classified as Class II medical devices and are listed under the FDA’s 510(k) pathway. Beech Medical, Inc. is headquartered in the United States.
Catalogue
Infusion Pump Ref K831089
Regimes: 510(k) Registry: 510(k)Beech Prolok Ref K933732
Regimes: 510(k) Registry: 510(k)Mini-Vol Extension Set Ref K831087
Regimes: 510(k) Registry: 510(k)Benzing Retrograde Admin. Set Ref K823373
Regimes: 510(k) Registry: 510(k)Mini-Vol I.V. Set Ref K831088
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Beech Medical, Inc. have in the registry?
The registry currently lists 5 devices for Beech Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beech Medical, Inc.'s devices?
Among its 5 most recently registered devices, Beech Medical, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Beech Medical, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Beech Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Beech Medical, Inc. in the registry?
The most recently registered devices listed for Beech Medical, Inc. include INFUSION PUMP, BEECH PROLOK, MINI-VOL EXTENSION SET and BENZING RETROGRADE ADMIN. SET.