Omeq Medical, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Omeq Medical, Ltd. makes
Omeq Medical, Ltd. manufactures the EpiFinder, a device designed for identifying and locating epinephrine auto-injectors in emergency situations, ensuring rapid access during anaphylaxis treatment.
The EpiFinder is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
EpiFinder Ref K221974
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omeq Medical, Ltd. have in the registry?
The registry currently lists 1 device for Omeq Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omeq Medical, Ltd.'s devices?
Among its 1 most recently registered device, Omeq Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Omeq Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Omeq Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omeq Medical, Ltd. in the registry?
The most recently registered devices listed for Omeq Medical, Ltd. include EpiFinder.