CF Pharma Ireland Ltd
IE-MF-000004595 · Ireland · Kilkenny
CF Pharma Ireland Ltd is registered in the European database on medical devices as a manufacturer, with 99 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 99 |
|---|
Most frequent device types declared: Effigerm Wound Care 1000ml gel. Spanish and Portuguese Language, Effigerm Wound Care Hydrogel, Effigerm Wound Care Hydrogel 500ml with scew cap, Effigerm Wound Cleansing Gel 60ml, Effigerm Wound Wash 500ml liquid DE.IT.
Devices declared under this manufacturer
- Aluderm 60 ml Hydrogel
- Dermosept
- Dermosept 1000ml Liquid
- Dermosept 60ml Liquid
- Dermosept 60ml liquid sample
- Effigerm Wound Care
- Effigerm Wound Cleansing Gel
- Effigerm Wound Wash
- Granusept
- Granuskin Face & Body 60ml
- Mediforte Wund Spullosung 500ml
- Mediforte Wund Spullosung 60ml
Showing 12 of 99 declared devices.
Catalogue references include FP1443, FP1653, FP1808, FP1830, FP1859, FP1870.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 99 |
| Country of registration | Ireland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 99 |
|---|---|
| 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. CF Pharma Ireland Ltd was not found in either the U.S. or the Canadian register.