VIDRA a spol. s.r.o.
SK-MF-000005837 · Slovakia · Žilina
VIDRA a spol. s.r.o. is registered in the European database on medical devices as a manufacturer, with 61 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 61 |
|---|
Most frequent device types declared: Kompresy z netkaného textilu nesterilné, Lopatka vyšetrovacia, Obväz hydrofilný pletený nesterilný, Obväzy - elastické, fixačné, hadicové.
Devices declared under this manufacturer
- Gáza skladaná 90 cm x 100 m
- Kompresy z gázy 7,5 cm x 7,5 cm
- Kompresy z netkaného textilu nesterilné 10cm x 10cm
- Náplasť fixačná z textilu Lutraplast 2,5cm x 5m
- Náplasť fixačná z transparentnej fólie, hypoalergénna Lutrafilm 5cm x
- Náplasť fixačná z umelého hodvábu so silnou lepivosťou, hypoalergénna
- Obväz elastický krepový so sponkami 14cm x 5m
- Obväz elastický universal 10cm x 5m
- Obväz elastický universal 15cm x 5m
- Obväz hydrofilný pletený nesterilný 10cm x 5m
- Obväz hydrofilný pletený nesterilný 16cm x 10m
- Obväz vysokoelastický fixačný 12cm x 4m
Showing 12 of 61 declared devices.
Catalogue references include 101020092, 101020094, 101020102, 101020171, 101025030, 101030024.
European nomenclature codes declared: M0303010101, M050101, M030101, M020199, M0201010102, M0201020102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 61 |
| Country of registration | Slovakia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 61 |
|---|---|
| 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. VIDRA a spol. s.r.o. was not found in either the U.S. or the Canadian register.