Hrvatski zavod za transfuzijsku medicinu
HR-MF-000019208 · Croatia · Zagreb
Hrvatski zavod za transfuzijsku medicinu is registered in the European database on medical devices as a manufacturer, with 40 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 40 |
|---|
Most frequent device types declared: Abdominalni dren, Aspiracijski kateter, Intrauterini kateter, Redon dren, Set za kisik.
Among these devices, 40 are declared sterile.
Devices declared under this manufacturer
- Abdominalni dren Ch 26
- Aspiracijski kateter Ch 10
- Aspiracijski kateter Ch 16
- Aspiracijski kateter Ch 18
- Aspiracijski kateter Ch 20
- Aspiracijski kateter Ch 6
- Cijev za povezivanje
- Intrauterini kateter
- Redon dren Ch 16
- Set za transfuziju
- Urinski kateter - tip Nelaton, muški, Ch 10
- Urinski kateter - tip Nelaton, muški, Ch 18
Showing 12 of 40 declared devices.
Catalogue references include 02010011, 02170012, 02170019, 02200007, 02220005, 02250002.
European nomenclature codes declared: U01010502, A0601010499, A99, A03040199, U08020101, U08020180.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 40 |
| Country of registration | Croatia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. Hrvatski zavod za transfuzijsku medicinu was not found in either the U.S. or the Canadian register.