Harry Holms AB
SE-MF-000001907 · Sweden · Munkfors
Harry Holms AB is registered in the European database on medical devices as a manufacturer, with 43 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 43 |
|---|
Devices declared under this manufacturer
- Dentalbricka 185x185x32 6 fack + 1 finmaskigt
- Insatskorg till Container 400x236x30
- Insatskorg till Container 400x236x60
- Insatsställ för 8 Practipal, bred
- Insatsställ för 8 brickor
- Instrument Tray 450x210x60
- Instrument Tray SPRI III 250x170x70
- Instrument Tray fine mesh 310x210x40
- Instrument Tray fine mesh with lid 150x60x45
- Instrument Tube fine mesh ø50x400
- Lid for Instrument Tray 50426 450x210
- Lid for Instrument Tray SPRI II 340x250
Showing 12 of 43 declared devices.
Catalogue references include 50055, 50427, 705010, 705205, 705305, 705330.
European nomenclature codes declared: S010401.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 43 |
| Country of registration | Sweden |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 43 |
|---|---|
| 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. Harry Holms AB was not found in either the U.S. or the Canadian register.