Tefra Med, Inc.
Country not established
- Devices
- 1
What Tefra Med, Inc. makes
Tefra Med, Inc. makes medical devices such as the DELTA MULTIPLE NON RETURN CONNECTOR, which is a type of connector.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Delta Multiple Non Return Connector Ref K841106
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tefra Med, Inc. have in the registry?
The registry currently lists 1 device for Tefra Med, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tefra Med, Inc.'s devices?
Among its 1 most recently registered device, Tefra Med, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Tefra Med, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tefra Med, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tefra Med, Inc. in the registry?
The most recently registered devices listed for Tefra Med, Inc. include DELTA MULTIPLE NON RETURN CONNECTOR.