Ermis Medizintechnik
GermanyFDA applicant, unverified
- Devices
- 1
What Ermis Medizintechnik makes
Ermis Medizintechnik manufactures the ERMIS Sterilization Container System, a device designed for protecting and transporting sterilized medical instruments and supplies.
The company’s portfolio is regulated under FDA’s Class II designation and requires 510(k) clearance. The system is listed in the FDA’s 510(k) database.
Catalogue
Ermis Sterilization Container System Ref K123234
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ermis Medizintechnik have in the registry?
The registry currently lists 1 device for Ermis Medizintechnik. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ermis Medizintechnik's devices?
Among its 1 most recently registered device, Ermis Medizintechnik has devices listed in FDA 510(k) (1 device).
What risk classes do Ermis Medizintechnik's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ermis Medizintechnik's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ermis Medizintechnik in the registry?
The most recently registered devices listed for Ermis Medizintechnik include ERMIS STERILIZATION CONTAINER SYSTEM.