Vitaid, Ltd.
Country not established
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Agishi Ascites Pump Peritoneocaval Shunt Pump Ref K894794
Regimes: 510(k) Registry: 510(k)Selfcath Ref K901738
Regimes: 510(k) Registry: 510(k)Wire Reinforced Endotracheal Tube Ref K932647
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Univent Tube 7.0mm, 7.5mm, 8.0mm, 8.5mm, 9.0mm Ref K894337
Regimes: 510(k) Registry: 510(k)Laser Shielding Tube Ref K894669
Regimes: 510(k) Registry: 510(k)Phycon All Silicone Balloon Catheter Ref K894883
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vitaid, Ltd. have in the registry?
The registry currently lists 7 devices for Vitaid, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitaid, Ltd.'s devices?
Among its 7 most recently registered devices, Vitaid, Ltd. has devices listed in FDA 510(k) (7 devices).
What risk classes do Vitaid, Ltd.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Vitaid, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitaid, Ltd. in the registry?
The most recently registered devices listed for Vitaid, Ltd. include AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP, SELFCATH, WIRE REINFORCED ENDOTRACHEAL TUBE and PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBES.