Blue Egg CO
South KoreaFDA applicant, unverified
- Devices
- 1
What Blue Egg CO makes
Blue Egg CO manufactures the UNIMOM ALLEGRO, a medical device designed for [specific application or use not provided in data]. This product is intended for [brief functional context, e.g., 'assisting in [procedure/condition]'] without further detail on its exact purpose.
The UNIMOM ALLEGRO is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Unimom Allegro Ref K100929
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Blue Egg CO have in the registry?
The registry currently lists 1 device for Blue Egg CO. Devices recorded under merged duplicate company entries are counted once.
Which registries list Blue Egg CO's devices?
Among its 1 most recently registered device, Blue Egg CO has devices listed in FDA 510(k) (1 device).
What risk classes do Blue Egg CO's devices fall under?
Among its 1 most recently registered device, the classes recorded for Blue Egg CO's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Blue Egg CO in the registry?
The most recently registered devices listed for Blue Egg CO include UNIMOM ALLEGRO.