Dimeda Instrumente GmbH
GermanyFDA applicant, unverified FDA FEI 3002806816
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
Dimela Obsterical Forceps, Model 72.1 Xx Xx Ref K092827
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3002806816
- DUNS number
- 317327724
- Address
- GANSACKER 54 + 58, TUTTLINGEN Baden-Wurttemberg
Frequently asked questions
How many devices does Dimeda Instrumente GmbH have in the registry?
The registry currently lists 2 devices for Dimeda Instrumente GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dimeda Instrumente GmbH's devices?
Among its 2 most recently registered devices, Dimeda Instrumente GmbH has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Dimeda Instrumente GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dimeda Instrumente GmbH's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dimeda Instrumente GmbH in the registry?
The most recently registered devices listed for Dimeda Instrumente GmbH include WESTCOTT Scissors 09.102.11 and DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX.