Transinternational Marketing Group
Country not established
- Devices
- 1
What Transinternational Marketing Group makes
Transinternational Marketing Group manufactures the Albert Morton Urological Catheter, a sterile, single-use device designed for urinary drainage in clinical settings.
The company’s portfolio is regulated under FDA Class II devices, with the Albert Morton Urological Catheter listed in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Albert Morton Urological Catheter Ref K901441
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Transinternational Marketing Group have in the registry?
The registry currently lists 1 device for Transinternational Marketing Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Transinternational Marketing Group's devices?
Among its 1 most recently registered device, Transinternational Marketing Group has devices listed in FDA 510(k) (1 device).
What risk classes do Transinternational Marketing Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Transinternational Marketing Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Transinternational Marketing Group in the registry?
The most recently registered devices listed for Transinternational Marketing Group include ALBERT MORTON UROLOGICAL CATHETER.