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, Respiratory and Anaesthesia devices, Snare.
Among these devices, 36 are declared sterile.
Devices declared under this manufacturer
- APL2002/1 Set mit Anstechdorn
- APL2002/26 Set Spirale und 1,2 Filter
- APL2002/34 Set Spiral, Y w Luer+RV, 0,2
- APL2002/4 Set m. 150 ml Res. u. 0,2 Filt
- LL 2012/22 Set mit Luer
- LL 2012/25 Set Spiral, Y w Luer+RV, 1,2
- LL 2012/3 mit 150 ml Reservoir
- LL 2012/34 Set Spiral, Y w Luer+RV, 0,2
- LL 2012/4 Set m. 150 ml Res. u. 0,2 Fil
- LL 2012/5 Set m gelber Leitung + 0,2 Fil
- LL 2012/6 Set m Y-Stück + 2. Leitung
- LL 2012/9 Set mit Anstechdorn u. 1,2 Fi
Showing 12 of 36 declared devices.
Catalogue references include 147305, 147315, 52026, 52034, 73016, 73022.
European nomenclature codes declared: A03040199, C019005, A070199, R028001.
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 |
Device-level evidence
| Devices with a numeric GTIN | 36 |
|---|---|
| Found in the U.S. device database | 7 |
| Share | 19.4 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: United States only. PFM medical mepro GmbH is registered in the United States but was not found in the Canadian register.