Teva Medical, Ltd.
Country not established
- Devices
- 2
What Teva Medical, Ltd. makes
Teva Medical, Ltd. manufactures injectable medications, including glatiramer acetate for subcutaneous use, and safety devices for syringes, such as the Free Flow Safety Device (Model MG 245052). Their portfolio includes pre-filled syringes designed for shared solution administration and needle safety mechanisms to reduce exposure risk.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company operates from the United States, adhering to U.S. regulatory requirements for medical devices.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Free Flow Safety Device, Model Mg 245052 Ref K990288
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Teva Medical, Ltd. have in the registry?
The registry currently lists 2 devices for Teva Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Teva Medical, Ltd.'s devices?
Among its 2 most recently registered devices, Teva Medical, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Teva Medical, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Teva Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Teva Medical, Ltd. in the registry?
The most recently registered devices listed for Teva Medical, Ltd. include COPAXONE (GLATIRAMER ACETATE FOR INJECTION) EZ-JECT FROM SHARED SOLUTIONS and FREE FLOW SAFETY DEVICE, MODEL MG 245052.