DMED DI D IMPRIMA ANGELO
IT-MF-000032812 · Italy · LORIA
DMED DI D IMPRIMA ANGELO is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Most frequent device types declared: Decontamination Washer, SEB100, SEB1000 - Smart Endo Box, SEB2000 - Automatic Endoscope Cleaning.
Devices declared under this manufacturer
- DW100
- DW15
- GANDY AEPS 10G
- SEB100 - Endoscope Flushing Aid
- SEB1000 Smart Endo BOX
- SEB2000 - automatic endoscope cleaning
Catalogue references include DW100, DW15, ETC 50, ETC 50S, ETC 70, ETC 70S.
European nomenclature codes declared: Z12011301, Z12029003, Z12011301,Z12011306, Z12011302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. DMED DI D IMPRIMA ANGELO was not found in either the U.S. or the Canadian register.