MP Biomedicals Germany GmbH
DE-MF-000020991 · Germany · Eschwege
MP Biomedicals Germany GmbH is registered in the European database on medical devices as a manufacturer, with 53 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: Various MP Rapid DOA/Alcohol Test Cassettes in different cut-offs, Various MP Rapid Drugs of Abuse Test Strips with different cut-offs.
Devices declared under this manufacturer
- Diagnostic Kit for CK-MB
- Diagnostic Kit for Free T3
- Diagnostic Kit for Myoglobin (Myo)
- Diagnostic Kit for PRL
- Diagnostic Kit for Procalcitonin (PCT)
- Diagnostic Kit for T4
- MP Rapid Drugs of Abuse Test Cup
- MP Rapid Drugs of Abuse/Alcohol Test Keyed Cup (Urine)
- Rapid Dengue NS1 Antigen Test Card
- Rapid SARS-CoV-2 Antigen Test Card
- Rapid SARS-CoV-2 Antigen Test Card (5 tests per box, NL)
- Rapid SARS-CoV-2 Influenza A+B Antigen Duo Test Card
Showing 12 of 53 declared devices.
Catalogue references include 07AG6001BSNL, 07AG6020FL, 07FT35025, 07MY5025, 07PCT5025, 07RD730701.
European nomenclature codes declared: W0105090501, W0102160511, W0105090199, W0105099004, W01020407, W0102160599.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 53 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 52 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
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: Neither register. MP Biomedicals Germany GmbH was not found in either the U.S. or the Canadian register.