HandyLegs B.V.
NL-MF-000023821 · Netherlands · Eemnes
HandyLegs B.V. is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Most frequent device types declared: HandyFix V2, HandyHold, HandyLegs V2, HandyOff, Size.
Devices declared under this manufacturer
- HandyFix
- HandyHold Extra Large
- HandyHold Extra extra large
- HandyHold Large
- HandyHold Medium
- HandyHold Small
- HandyLegs 1
- HandyLegs 2
- HandyLegs Large
- HandyLegs Medium
- HandyLegs Small
- HandyOff
Catalogue references include HandyFix V2, HandyHold S, HandyHold XL, HandyLegs 1 V2, HandyLegs 2 V2, HandyLegs Large.
European nomenclature codes declared: M030499, M030405.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| 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 | 12 |
|---|---|
| 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. HandyLegs B.V. was not found in either the U.S. or the Canadian register.