Cathaid, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Cathaid, Inc. makes
Cathaid, Inc. makes the Tubegripper, a urological catheter and accessory, as well as versions of the Tubegripper designed for drainage catheters and accessories used in SU and GU applications.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Tubegripper, Urological Catheter & Accessory Ref K863958
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cathaid, Inc. have in the registry?
The registry currently lists 3 devices for Cathaid, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cathaid, Inc.'s devices?
Among its 3 most recently registered devices, Cathaid, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Cathaid, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cathaid, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cathaid, Inc. in the registry?
The most recently registered devices listed for Cathaid, Inc. include TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY, TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU and TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR GU.