Vacutest Kima SRL
ItalyFDA applicant, unverified FDA FEI 3010280735
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Vacutest Kima SRL makes
Vacutest Kima Srl manufactures blood collection needles designed for venipuncture procedures, including those used in phlebotomy and laboratory diagnostics.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Blood Collection Needles Ref K200932
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3010280735
- Address
- VIA DELL'INDUSTRIA 12, ARZERGRANDE Padova
Frequently asked questions
How many devices does Vacutest Kima Srl have in the registry?
The registry currently lists 1 device for Vacutest Kima Srl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vacutest Kima Srl's devices?
Among its 1 most recently registered device, Vacutest Kima Srl has devices listed in FDA 510(k) (1 device).
What risk classes do Vacutest Kima Srl's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vacutest Kima Srl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vacutest Kima Srl in the registry?
The most recently registered devices listed for Vacutest Kima Srl include Blood Collection Needles.