Definitive Medical Technologies, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Definitive Medical Technologies, Ltd. makes
Definitive Medical Technologies, Ltd. manufactures the AFF (Mark I) volumetric infusion pump, a device designed for controlled delivery of fluids in medical settings.
The company’s portfolio is regulated under FDA Class II devices, with the AFF (Mark I) listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Aff (Mark I) Volumetric Infusion Pump Ref K070529
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Definitive Medical Technologies, Ltd. have in the registry?
The registry currently lists 1 device for Definitive Medical Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Definitive Medical Technologies, Ltd.'s devices?
Among its 1 most recently registered device, Definitive Medical Technologies, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Definitive Medical Technologies, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Definitive Medical Technologies, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Definitive Medical Technologies, Ltd. in the registry?
The most recently registered devices listed for Definitive Medical Technologies, Ltd. include AFF (MARK I) VOLUMETRIC INFUSION PUMP.