Molnlycke Clinical Products AB
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mepitel Non-Adherent Silicone Dressing Ref K914604
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Molnlycke Clinical Products AB have in the registry?
The registry currently lists 1 device for Molnlycke Clinical Products AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Molnlycke Clinical Products AB's devices?
Among its 1 most recently registered device, Molnlycke Clinical Products AB has devices listed in FDA 510(k) (1 device).
What risk classes do Molnlycke Clinical Products AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Molnlycke Clinical Products AB's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Molnlycke Clinical Products AB in the registry?
The most recently registered devices listed for Molnlycke Clinical Products AB include MEPITEL NON-ADHERENT SILICONE DRESSING.