Lola Ribar d.o.o. za proizvodnju saniteta
HR-MF-000018260 · Croatia · Zagreb
Lola Ribar d.o.o. za proizvodnju saniteta is registered in the European database on medical devices as a manufacturer, with 242 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 242 |
|---|
Most frequent device types declared: LOLAAQUA 10X20cm upojni vodootporni flaster, LOLAAQUA 10X25cm upojni vodootporni flaster.
Among these devices, 20 are declared sterile.
Devices declared under this manufacturer
- GAZA NESTERILNA 80 CM X 100 M 7/6
- KOMPRESE NESTERILNE 7,5X7,5 16 SL A5 A100 ŠLAJFANE
- KOMPRESE NESTERILNE 5 X 5 16 SL. Á100 KOM
- KREP ZAVOJ 12CM X 10M
- KREP ZAVOJ 15CM X 5 M
- LOLA CARE -KALIKO ZAVOJ S UTKANIM RUBOM 8 CM X 4M
- LOLAAQUA 10X25cm upojni vodootporni flaster
- LOLALAST ELASTIČNI ZAVOJ 15CM X 4M
- NETKANE NESTERILNE KOMPRESE 10CM X 10CM 4 SL A100 KOM
- NETKANE NESTERILNE KOMPRESE 5CM X 5CM 6 SL A100 KOM
- STANIČEVINA U ROLI 60CM X 80M
- ZAVOJ - MUL REZANI RUB 20 CM X 5 M
Showing 12 of 242 declared devices.
Catalogue references include 1213, 1402, 1414, 1569, 1685, 1845.
European nomenclature codes declared: M0201020102, M0299, M030101, M03030103, M0202010102, H900299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 242 |
| Country of registration | Croatia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 242 |
|---|---|
| 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. Lola Ribar d.o.o. za proizvodnju saniteta was not found in either the U.S. or the Canadian register.