GP Medical Devices A/S
DK-MF-000022391 · Denmark · Holstebro
GP Medical Devices A/S is registered in the European database on medical devices as a manufacturer, with 21 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 1 |
|---|
Most frequent device types declared: 10, 12, 13, 14, 15.
Devices declared under this manufacturer
- EasyDrainer drainage sleeve
- EasySampler Basic
- EasySampler Basic Complete Stool Collection Kit
- EasySampler Basic DRS
- EasySampler Basic bulk
- EasySampler Complete Stool Collection Kit Triple
- EasySampler Mini Kit - Single
- EasySampler Mini Kit - Single US
- EasySampler Mini Kit - Triple
- EasySampler Stool Collector - Single
- EasySampler Stool Collector Bulk
- EasySampler urine collector
Showing 12 of 21 declared devices.
Catalogue references include 10 60 10, 10 60 30, 10 70 30, 12 60 10, 13 01 00, 13 70 00.
European nomenclature codes declared: W05019001, W05010299,W05019001, W05019099, A0699.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | GP MEDICAL DEVICES A/S (DK) · FDA 3010162618 |
| Devices in EUDAMED | 21 |
| Country of registration | Denmark |
Device-level evidence
| Devices with a numeric GTIN | 21 |
|---|---|
| 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: United States only. GP Medical Devices A/S is registered in the United States but was not found in the Canadian register.