PK Benelux BV
NL-MF-000006672 · Netherlands · Uden
PK Benelux BV is registered in the European database on medical devices as a manufacturer, with 505 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 505 |
|---|
Devices declared under this manufacturer
- Amazon Fungal Nail 10 ml
- BEAVITA Sättigungskapseln
- Dr. Gut IBS 15 caps
- Drenax Grassi Max 45 t
- Etos vaginale gel
- Femidoc D-man to go
- Fungimax Athlete’s foot gel
- Health Routine Nagelpilz Lösung
- HealthAid IBS
- Kapseln gegen Durchfall 30 c
- Sabora Pharma Oy D-Ma
- Urimenna kapszula 30 c
Showing 12 of 505 declared devices.
Catalogue references include 073385, 074924, 075624, 17983107, 21994, 315337.
European nomenclature codes declared: G0402, G0401, V9099, G0499, M9002, M04041503.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 505 |
| 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 | 1 |
|---|---|
| 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. PK Benelux BV was not found in either the U.S. or the Canadian register.