Duopross Meditech Corporation
Country not established FDA establishment FEI 3003681915
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Duopross Meditech Corporation makes
Duopross Meditech Corporation manufactures disposable medical needles and syringes designed for single-use injections and fluid administration in clinical settings.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
DuoprossTM Smart Cap (Type I) Ref K252518
510(k) 510(k)Duopross Needle Ref K052445
510(k) 510(k)Duopross Syringes Ref K042500
510(k) 510(k)
Company details
- FDA FEI number
- 3003681915
- Address
- 154 Marine St, FARMINGDALE, NY, 11735
Frequently asked questions
How many devices does DUOPROSS MEDITECH CORPORATION have in the registry?
The registry currently lists 3 devices for DUOPROSS MEDITECH CORPORATION. Devices recorded under merged duplicate company entries are counted once.
Which registries list DUOPROSS MEDITECH CORPORATION's devices?
Among its 3 most recently registered devices, DUOPROSS MEDITECH CORPORATION has devices listed in FDA 510(k) (3 devices).
What risk classes do DUOPROSS MEDITECH CORPORATION's devices fall under?
Among its 3 most recently registered devices, the classes recorded for DUOPROSS MEDITECH CORPORATION's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from DUOPROSS MEDITECH CORPORATION in the registry?
The most recently registered devices listed for DUOPROSS MEDITECH CORPORATION include DuoprossTM Smart Cap (Type I), DUOPROSS NEEDLE and DUOPROSS SYRINGES.