Temed
United KingdomFDA applicant, unverified FDA FEI 3014247825
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Temed makes
Temed manufactures blood tubing sets designed for cardiopulmonary bypass systems, ensuring safe and efficient circulation during surgical procedures. The company also produces surgical wound gas diffusers, which facilitate oxygen therapy for open wounds.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI registries. Temed operates from the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
TEMED Gas Diffuser Ref K173545
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3014247825
- DUNS number
- 215842226
- Address
- Unit 3 Keynor Farm, Sidlesham West Sussex
- [email protected]
- Phone
- +441243572255
Frequently asked questions
How many devices does Temed have in the registry?
The registry currently lists 4 devices for Temed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Temed's devices?
Among its 4 most recently registered devices, Temed has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Temed's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Temed's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Temed in the registry?
The most recently registered devices listed for Temed include TEMED P2525, TEMED P2524, TEMED P2514 and TEMED Gas Diffuser.