Germo SpA
IT-MF-000029930 · Italy · Cormano (MI)
Germo SpA is registered in the European database on medical devices as a manufacturer, with 51 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 37 |
|---|---|
| Class IIb | 14 |
Most frequent device types declared: DETERGENTE CONCENTRATO STRUMENTI, DISINFETTANTE DETERGENTE A BASE DI ALDEIDE GLUTARICA, DISINFETTANTE DETERGENTE AD ALTO CONTENUTO ALCOLICO, DISINFETTANTI DETERGENTI ALCOHOL FREE, DISINFETTANTI DETERGENTI A BASSO CONTENUTO ALCOLICO.
Devices declared under this manufacturer
- GD STERIXIDINA5
- GD ENZIMATICO10
- GERMOCID BASIC
- GERMOCID BASIC WIPES
- GERMOCID INSTRUMENTS
- GERMOCID WIPES
- IGOSAFE NEO INSTRUMENTS
- INSTRUMENT DISINFECTION PREMIUM
- LACLEDIN SUPERFICIES/SURFACE
- NEW SPRAYGEN
- PHARMASTERIL SPRAY 2.0
- PURA ENZIMATICO CONCENTRATO
Showing 12 of 51 declared devices.
Catalogue references include A857, B391, D101, D102, L007, R612.
European nomenclature codes declared: D0902, D020199, D0801, D010199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 51 |
| 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 | 51 |
|---|---|
| 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. Germo SpA was not found in either the U.S. or the Canadian register.