Elers Medical Finland Oy
FI-MF-000007877 · Finland · Espoo
Elers Medical Finland Oy is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: Type I, Type II, Type IIR.
Devices declared under this manufacturer
- Disposable Surgical Face Mask (Type II) with earloop, (non sterile), b
- Disposable Surgical Face Mask (Type IIR) with earloop, (non-sterile),
- Disposable face mask (Type I) with earloop, (non sterile), blue
- Disposable surgical face mask (Type IIR) with earloop, (non sterile),
- Disposable surgical face mask (Type IIR) with tieback anti-fog, (non s
- Disposable surgical face mask (Type IIR) with tieback, (non sterile),
- ELERS MEDICAL® Indurate®
Catalogue references include B102, EMCS, M-102, M007, M025, N102.
European nomenclature codes declared: T020604, T020603, Q010699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| 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. Elers Medical Finland Oy was not found in either the U.S. or the Canadian register.