B. Braun Medical AG
CH-MF-000017781 · Switzerland · Sempach
B. Braun Medical AG is registered in the European database on medical devices as a manufacturer, with 84 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 77 |
|---|---|
| Class IIb | 7 |
Among these devices, 13 are declared sterile.
Authorised representative in the Union: B. Braun Melsungen AG.
Devices declared under this manufacturer
- B.Braun
- Helimatic®
- Helipur®
- Helizyme®
- Meliseptol®
- Prontosan®
- Stabimed®
- Uro-Tainer®
Showing 12 of 84 declared devices.
Catalogue references include 180350, 180388, 18676, 18823, 19804, 19828.
European nomenclature codes declared: V0799, D0799, D0701, U0180, D01010102, D0902.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | B. BRAUN MEDICAL AG (CH) · FDA 8031007 |
| Devices in EUDAMED | 84 |
| Country of registration | Switzerland |
Device-level evidence
| Devices with a numeric GTIN | 84 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | B. BRAUN MEDICAL INC. |
North American profile: Both markets. B. Braun Medical AG is registered in both the United States and Canada.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G15 061585 0043 | supplemented | 2031-03-14 |