Mediziv Medical Devices, Ltd.
IsraelFDA applicant, unverified
- Devices
- 2
What Mediziv Medical Devices, Ltd. makes
Mediziv Medical Devices, Ltd. manufactures epidural infusion systems for pain management and central venous catheters for intravenous access and fluid administration.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Mediziv Epidural Systems Ref K894725
Regimes: 510(k) Registry: 510(k)Mediziv Central Vein Catheter Ref K884491
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mediziv Medical Devices, Ltd. have in the registry?
The registry currently lists 2 devices for Mediziv Medical Devices, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediziv Medical Devices, Ltd.'s devices?
Among its 2 most recently registered devices, Mediziv Medical Devices, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mediziv Medical Devices, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mediziv Medical Devices, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mediziv Medical Devices, Ltd. in the registry?
The most recently registered devices listed for Mediziv Medical Devices, Ltd. include MEDIZIV EPIDURAL SYSTEMS and MEDIZIV CENTRAL VEIN CATHETER.