PFM medical mepro GmbH
DE-MF-000005190 · Germany · Nonnweiler-Otzenhausen
PFM medical mepro GmbH is registered in the European database on medical devices as a manufacturer, with 36 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 36 |
|---|
Most frequent device types declared: Infusionsset, Snare, Respiratory and Anaesthesia devices.
Among these devices, 36 are declared sterile.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | pfm medical mepro gmbh (DE) · FDA 3005704822 |
| Devices in EUDAMED | 36 |
| Country of registration | Germany |