Ultrasun International B.V.
NetherlandsFDA applicant, unverified
- Devices
- 8
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
i8 Tanning Booth Ref K210004
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 403421761
Frequently asked questions
How many devices does Ultrasun International B.V. have in the registry?
The registry currently lists 8 devices for Ultrasun International B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultrasun International B.V.'s devices?
Among its 8 most recently registered devices, Ultrasun International B.V. has devices listed in FDA 510(k) (1 device) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Ultrasun International B.V.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Ultrasun International B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultrasun International B.V. in the registry?
The most recently registered devices listed for Ultrasun International B.V. include Ultrasun E6 1V16D304AC842, Ultrasun Q6-0 1V26D304AC842, Ultrasun Q6-2 Magnum Power 1V27D304BC842 and Ultrasun Q10-0 1V30D314AC443.