Medex Instrumenten Service
NL-MF-000010798 · Netherlands · Almere
Medex Instrumenten Service is registered in the European database on medical devices as a manufacturer, with 773 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 773 |
|---|
Among these devices, 25 are declared reusable.
Devices declared under this manufacturer
- Borenhouder POM/RVS tbv 14 Bien Air boortjes 70mm
- Dilatator tbv urologie (urethra) 6mm
- Gipsschaar HM Bruns 23cm met veer
- Instrumentfixatie in RVS mand MFS25-032
- Instrumentfixatie in RVS mand MFS25-064
- Instrumentfixatie in RVS mand MFS25-198
- Instrumentfixatie in RVS mand MFS25-214
- Instrumentfixatie in RVS mand MFS25-256
- Instrumentfixatie in RVS mand MFS25-309
- Instrumentfixatie in RVS mand MFS26-001
- Instrumentfixatie in RVS mand MFS26-049
- Instrumentfixatie in RVS mand MFS26-064
Showing 12 of 773 declared devices.
Catalogue references include ME00-226, ME00-244-14, ME27-170V, MFS25-256, MFS25-309, MFS26-001.
European nomenclature codes declared: S010401, V9099, L03140104, A070199, L06050101, L149003.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 773 |
| 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 | 773 |
|---|---|
| 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. Medex Instrumenten Service was not found in either the U.S. or the Canadian register.