Medinovitas Kft
HU-MF-000007416 · Hungary · Hajdúböszörmény
Medinovitas Kft is registered in the European database on medical devices as a manufacturer, with 111 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 111 |
|---|
Most frequent device types declared: Benda elastica previcrepe.
Devices declared under this manufacturer
- Benda di garza orlata 10mx6cm
- Benda elastica previcrepe 4cmx4m
- Benda elastica previcrepe L 4,5mx20cm
- Benda elastica previcrepe L 4,5mx6cm
- Benda elastica previcrepe L 4cmx4m
- Benda prevideal nuda con clips 4mx15cm
- Benda previfix nuda s/clip 4mx6cm
- Benda previgarzelast CV nuda 4mx4cm
- Benda previlast 4mx4cm
- Benda previlast nuda s/clip 4mx4cm
- Benda previlast s/clip 4mx8cm
- Benda previmedical nuda 10pz 5mx12cm
Showing 12 of 111 declared devices.
Catalogue references include 23F100061L, CREL0450631, CREL0452032, GACO2000810FL, GACV04004, LAS04004.
European nomenclature codes declared: M0303010101, M0304010103, M030101, M0303010201, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 111 |
| Country of registration | Hungary |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 111 |
|---|---|
| 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. Medinovitas Kft was not found in either the U.S. or the Canadian register.