Avery Dennison Medical
IE-MF-000001926 · Ireland · Longford
Avery Dennison Medical is registered in the European database on medical devices as a manufacturer, with 19 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 19 |
|---|
Among these devices, 2 are declared sterile.
Devices declared under this manufacturer
- Ally Barrier Film Spray
- Askina Barrier Cream
- Askina Barrier Film Spray
- Askina Barrier Film Swab
- Hartmann MedProtect Barrier Film Swab
- Hartmann MedProtect barrier cream
- Hartmann MedProtect barrier film Spray
- Onyster® Polyurethane Film Nail Plaster
- Superfiller
Showing 12 of 19 declared devices.
Catalogue references include 22214, 5036, 5038, F05008C, F05008F, MED L120450.
European nomenclature codes declared: M9002, A108001, A108005, Z12011399, M0599.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Avery Dennison Medical Ltd. (IE) · FDA 3006506075 |
| Devices in EUDAMED | 19 |
| Country of registration | Ireland |
Device-level evidence
| Devices with a numeric GTIN | 19 |
|---|---|
| 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: United States only. Avery Dennison Medical is registered in the United States but was not found in the Canadian register.