Angiplast Private, Ltd.
IndiaFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Angeltouch Vented Iv Administration Set Ref K012189
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Angiplast Private, Ltd. have in the registry?
The registry currently lists 2 devices for Angiplast Private, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angiplast Private, Ltd.'s devices?
Among its 2 most recently registered devices, Angiplast Private, Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Angiplast Private, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Angiplast Private, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angiplast Private, Ltd. in the registry?
The most recently registered devices listed for Angiplast Private, Ltd. include ANGELTOUCH IT-04 and ANGELTOUCH VENTED IV ADMINISTRATION SET.