Lomed Nederland
NL-MF-000032807 · Netherlands · 's-Hertogenbosch
Lomed Nederland is registered in the European database on medical devices as a manufacturer, with 234 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 234 |
|---|
Most frequent device types declared: APA SP EZBT0, APA SP W-51008, AW PO 1106, PO 31161, PO 31306.
Devices declared under this manufacturer
- Airwalker Pro-Orthic Maat S
- Buddy splint 50 mm
- Epi Comfort
- Epi Comfort - M
- Genu Comfort - XL
- Joint 8
- Malleo Lacer - L
- Malleo Lacer - M
- Polsbrace 8'' Rechts L
- Posturex - L
- Rib band
- TFCC Brace Beige
Showing 12 of 234 declared devices.
Catalogue references include APA SP W-51008, AW PO 1106 S, PO 31161 L, PO 31306, PO 31306 M, PO 31423 S.
European nomenclature codes declared: Y060612, Y060603, Y061209, Y06120601, M03040199, Y060615.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 234 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 234 |
|---|---|
| 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. Lomed Nederland was not found in either the U.S. or the Canadian register.