Will-Pharma BV
NL-MF-000006884 · Netherlands · Schiphol-Rijk
Will-Pharma BV is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 12 |
|---|---|
| Class I | 15 |
Most frequent device types declared: Willocell Fibril, Willocell Knit, Willocell Standard, Willomesh®.
Among these devices, 27 are declared sterile, 27 implantable.
Devices declared under this manufacturer
- Willocell
- Willomesh
- Willomesh®
- Willospon®
- Willospon® Dental
- Willospon® Special
- Willospon® Tampon
Showing 12 of 27 declared devices.
Catalogue references include 26013NL-05, 26014NL-05, 26017NL-05, 26018NL-01, 26019NL-05, 26020NL-05.
European nomenclature codes declared: P900202, M040504, M040503.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| 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 | 27 |
|---|---|
| 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. Will-Pharma BV was not found in either the U.S. or the Canadian register.