Handinor USA, Inc.
Country not established
- Devices
- 1
What Handinor USA, Inc. makes
Handinor USA, Inc. manufactures the HANDIVIPP, a device designed for intravenous catheter insertion and management, including secure attachment and stabilization of peripheral lines.
The HANDIVIPP is classified as a Class I medical device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Handivipp Ref K033125
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Handinor USA, Inc. have in the registry?
The registry currently lists 1 device for Handinor USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Handinor USA, Inc.'s devices?
Among its 1 most recently registered device, Handinor USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Handinor USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Handinor USA, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Handinor USA, Inc. in the registry?
The most recently registered devices listed for Handinor USA, Inc. include HANDIVIPP.