Rudolf Medical GmbH + Co. KG
GermanyFDA applicant, unverified FDA FEI 3003448211
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Rudolf Medical GmbH + Co. KG makes
Rudolf Medical GmbH + Co. KG makes laparoscopic and electrosurgical instruments and accessories, including the Laparoscopy Rudolf System. These products are used in medical procedures.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510k registry. The company is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003448211
- Address
- ZOLLERSTRASSE 1, FRIDINGEN Baden-Wurttemberg
Frequently asked questions
How many devices does Rudolf Medical GmbH + Co. KG have in the registry?
The registry currently lists 1 device for Rudolf Medical GmbH + Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rudolf Medical GmbH + Co. KG's devices?
Among its 1 most recently registered device, Rudolf Medical GmbH + Co. KG has devices listed in FDA 510(k) (1 device).
What risk classes do Rudolf Medical GmbH + Co. KG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rudolf Medical GmbH + Co. KG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rudolf Medical GmbH + Co. KG in the registry?
The most recently registered devices listed for Rudolf Medical GmbH + Co. KG include LAPAROSCOPIC AND ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, LAPAROSCOPY RUDOLF SYSTEM.