QLRAD international Ltd
NL-MF-000012167 · Netherlands · Almere
QLRAD international Ltd is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Most frequent device types declared: 105.1001, 105.1014, 105.1018, 105.2000, 105.3000.
Among these devices, 1 are declared reusable.
Devices declared under this manufacturer
- RectalPro75
- Skin fold Breast Wedge
Catalogue references include 105.1001, 105.1014, 105.1018, 105.2000, 105.3000.
European nomenclature codes declared: G0301010501, T030499, V0804.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| Found in the U.S. device database | 5 |
| Share | 100.0 % |
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. QLRAD international Ltd was not found in either the U.S. or the Canadian register.