Urethrotech
Active in EUDAMEDUnited Kingdomfrom SRN EUDAMED FDA SRN UK-MF-000043649 FEI 3016738724
- Devices
- 3
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
What Urethrotech makes
Urethrotech manufactures the Urethrotech UCD, which is a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
Ucd Ref UCD-0035-090-0016
CE MDR EUDAMEDUcd Ref UCD-0035-090-0014
CE MDR EUDAMEDUrethrotech UCD Ref K190060
510(k) 510(k)
Company details
- EUDAMED SRN
- UK-MF-000043649
- FDA FEI number
- 3016738724
- EU VAT number
- GB 144772891
- EUDAMED status
- Active
- EUDAMED registered name
- Urethrotech Ltd
- EUDAMED abbreviated name
- Urethrotech
- Registered address
- 24, Garth Road, KT2 5NY, Kingston upon Thames, United Kingdom (ex Northern Ireland)
- Website
- www.urethrotech.com
- [email protected]
- Phone
- +44-800-0517219
- PRRC contact
- Andrew Micklethwaite
Frequently asked questions
How many devices does Urethrotech have in the registry?
The registry currently lists 3 devices for Urethrotech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Urethrotech's devices?
Among its 3 most recently registered devices, Urethrotech has devices listed in EUDAMED (2 devices) and FDA 510(k) (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Urethrotech's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Urethrotech's devices are Class IIa and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Urethrotech in the registry?
The most recently registered devices listed for Urethrotech include UCD and Urethrotech UCD.