ADRANOX SRL
IT-MF-000027181 · Italy · MANTOVA
ADRANOX SRL is registered in the European database on medical devices as a manufacturer, with 63 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 49 |
|---|---|
| Class IIb | 14 |
Most frequent device types declared: ADMR100.10, ADMR102.10, ADMR201.075, ADWD300.50.
Devices declared under this manufacturer
- LYSONOX BIOWIPES ACTIVE
- LYSONOX D1
- LYSONOX DECON FX
- LYSONOX ENZY4CLEAN PLUS
- LYSONOX INSTRUMENTS DR
- LYSONOX N
- LYSONOX PAA
- LYSONOX R
- LYSONOX S10
- LYSONOX STEELMAXX
- LYSONOX TERGO EXTRA
- LYSONOX WD POWDER
Showing 12 of 63 declared devices.
Catalogue references include AD004MR, AD005WDL, ADMR100.10, ADMR11, ADMR200.10, ADMR201.075.
European nomenclature codes declared: V0799, D99, D050199, D0599, S9002, D0801.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 63 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 63 |
|---|---|
| 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. ADRANOX SRL was not found in either the U.S. or the Canadian register.