Mascia Brunelli S.p.A.
IT-MF-000009572 · Italy · Milano
Mascia Brunelli S.p.A. is registered in the European database on medical devices as a manufacturer, with 127 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 1 |
|---|
Most frequent device types declared: HEMOFAST, STROMATOL.
Among these devices, 8 are declared sterile, 1 implantable.
Devices declared under this manufacturer
- CAMPYLOBACTER AGAR BLASER WANG
- CHOCOLATE AGAR ENRICHED
- CHROMART ESBL
- COLOREX ACINETOBACTER
- COLUMBIA BLOOD AGAR
- DERMATOPHYTE TEST MEDIUM/SABOURAUD DEXTROSE AGAR + CAF
- HEKTOEN ENTERIC AGAR
- LEGIONELLA AGAR BASE (BCYE)
- LEVINE EMB BLUE AGAR
- MUELLER HINTON AGAR II
- NUTRIENT AGAR
- TRIPLE SUGAR IRON AGAR
Showing 12 of 127 declared devices.
Catalogue references include 501740P, 5118102, 541111, 541136, 541541, 548020.
European nomenclature codes declared: W0104010405, W0104010402, W0104010604, W0104010306, W0104030299, W0104010206.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 127 |
| 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 | 127 |
|---|---|
| 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. Mascia Brunelli S.p.A. was not found in either the U.S. or the Canadian register.