Prodimed
Country not established FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Prodimed makes
Prodimed manufactures microinjection pipettes used for laboratory procedures.
The company is based in the US, and its products are classified as Class II medical devices listed in the FDA 510(k) registry.
Catalogue
Prodimed Microinjection Pipettes Ref K983713
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Prodimed NEUILLY-EN-THELLE Oise · FR FEI 3002807433
Frequently asked questions
How many devices does Prodimed have in the registry?
The registry currently lists 1 device for Prodimed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prodimed's devices?
Among its 1 most recently registered device, Prodimed has devices listed in FDA 510(k) (1 device).
What risk classes do Prodimed's devices fall under?
Among its 1 most recently registered device, the classes recorded for Prodimed's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Prodimed in the registry?
The most recently registered devices listed for Prodimed include PRODIMED MICROINJECTION PIPETTES.
Which FDA establishments are linked to Prodimed?
1 FDA establishment is linked to Prodimed in the registry; they are listed on the company page.