Rotec Medizintechnik GmbH
GermanyFDA applicant, unverified
- Devices
- 2
What Rotec Medizintechnik GmbH makes
Rotec Medizintechnik GmbH manufactures medical devices including the MRP-TITAN and MRS-TITAN, which are Class II devices.
The company's products are listed in the FDA 510(k) registry and the company is based in the US.
Catalogue
Frequently asked questions
How many devices does Rotec Medizintechnik GmbH have in the registry?
The registry currently lists 2 devices for Rotec Medizintechnik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rotec Medizintechnik GmbH's devices?
Among its 2 most recently registered devices, Rotec Medizintechnik GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Rotec Medizintechnik GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Rotec Medizintechnik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rotec Medizintechnik GmbH in the registry?
The most recently registered devices listed for Rotec Medizintechnik GmbH include MRP-TITAN and MRS-TITAN.