Mequ A/S
DenmarkFDA applicant, unverified FDA FEI 3032580628
- Devices
- 8
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
°M Warmer System Ref K232107
Regimes: 510(k) Registry: 510(k)°M Warmer System with °M Station Ref K260988
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3032580628
- Address
- Fruebjergvej 3, Copenhagen Hovedstaden
- Website
- www.mequ.dk
- linkedin.com/company/mequ
- facebook.com/Bloodwarmer
- [email protected]
Frequently asked questions
How many devices does MEQU A/S have in the registry?
The registry currently lists 8 devices for MEQU A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list MEQU A/S's devices?
Among its 8 most recently registered devices, MEQU A/S has devices listed in FDA 510(k) (2 devices) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do MEQU A/S's devices fall under?
Among its 8 most recently registered devices, the classes recorded for MEQU A/S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MEQU A/S in the registry?
The most recently registered devices listed for MEQU A/S include °M Warmer System - °M Station MWS405, °M Warmer System - °M Station MWS406, °M Warmer System - Starter Kit MWS005 and °M Warmer System - Power Pack MWS105.