Elysium Laboratories Kft.
HU-MF-000039543 · Hungary · Budapest
Elysium Laboratories Kft. is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 25 |
|---|
Devices declared under this manufacturer
- Elysium Cumi Doki Cumis gyógyszeradagoló készlet
- Elysium orrmosó - 300 ml (kék)
- Elysium orrmosó fecskendő béka fejjel
- Elysium orrmosó fecskendő csibe fejjel
- Elysium orrmosó fecskendő nyuszi fejjel
- Elysium orrmosó só 2,7g - 30 db
- Elysium szúnyog- és kullancsriasztó tapasz (0-3 éves korig) - dínós
- Elysium szúnyog- és kullancsriasztó tapasz (3 éves kor felett) - állat
- Elysium szúnyog- és kullancsriasztó tapasz (3 éves kor felett) - űrhaj
- HESS! Fém tetűfésű nagyítóval PP foglalatban
- HESS! Fémházas tetűfésű nagyítóval
- HESS! Kullancskiszedő kanál
Showing 12 of 25 declared devices.
Catalogue references include 10001, 10003, 10022, 10023, 10048, 5999862705022.
European nomenclature codes declared: V9099, Q030103, Z120499, V901001, Z12149099, A020299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 25 |
| 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 | 25 |
|---|---|
| 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. Elysium Laboratories Kft. was not found in either the U.S. or the Canadian register.