Msi Medserv International Deutschland GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Msi Medserv International Deutschland GmbH makes
Msi Medserv International Deutschland GmbH manufactures rigid endoscopes, which are used for visual inspection of internal body cavities and lumens in medical procedures. These devices are designed for diagnostic and therapeutic applications across various specialties, including gastroenterology, urology, and otolaryngology.
The company’s rigid endoscopes fall under Class II regulatory classification in the US, requiring premarket notification (510(k)) clearance through the FDA. These devices are listed in the FDA’s 510(k) database, adhering to US medical device regulations. The manufacturer operates from the United States.
Catalogue
Msi Medserv International-Rigid Endoscope Ref K083840
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Msi Medserv International Deutschland GmbH have in the registry?
The registry currently lists 1 device for Msi Medserv International Deutschland GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Msi Medserv International Deutschland GmbH's devices?
Among its 1 most recently registered device, Msi Medserv International Deutschland GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Msi Medserv International Deutschland GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Msi Medserv International Deutschland GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Msi Medserv International Deutschland GmbH in the registry?
The most recently registered devices listed for Msi Medserv International Deutschland GmbH include MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE.