B.P.C. BIOSED – S.R.L.
IT-MF-000032961 · Italy · CASTELNUOVO DI PORTO (RM)
B.P.C. BIOSED – S.R.L. is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Automated Biochemistry Analyzer GLOBAL 240
- Automated Biochemistry Analyzer GLOBAL 400
- Automated Biochemistry Analyzer GLOBAL 400 + ISE
- Automated Biochemistry Analyzer GLOBAL 4500DR
- Automated Biochemistry Analyzer GLOBAL 720
- Automated Biochemistry Analyzer GLOBAL 7500DR
- EXTRA CLEANING
- IPO CLEANING
- KENZA MAX PLUS BioChemisTry PHOTOMETER
- SOLEA QUICK - COAGULOMETER 1 CHANNEL, including accessories
Catalogue references include 19-G720, 22-0000, 22-DM400ISE, 22-DN400, 22-G7500DR, CO4020.
European nomenclature codes declared: W0201010106, W0103010105, W0201010102, W0201010101, W0202020101, W0201010105.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 10 |
|---|---|
| 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. B.P.C. BIOSED – S.R.L. was not found in either the U.S. or the Canadian register.