Rushwood b.v.
NL-MF-000005745 · Netherlands · Raamsdonksveer
Rushwood b.v. is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 10 |
|---|
Most frequent device types declared: 500 ml.
Devices declared under this manufacturer
- Gloup FEES 500ml
- Gloup Forte 25 x 8ml
- Gloup Forte 500ml
- Gloup Kids 150ml
- Gloup Original 150ml
- Gloup Original 25 x 8ml
- Gloup Original 500ml
- Gloup Original 75ml
- Gloup Zero 500ml
- Gloup Zero 75ml
Catalogue references include 02.02.F0500, 02.02.S0008, 02.02.T0075, 02.02.T0150, 02.03.F0500, 02.06.F0500.
European nomenclature codes declared: M9002.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | RUSHWOOD B.V. (NL) · FDA 3013774666 |
| Devices in EUDAMED | 10 |
| Country of registration | Netherlands |
Device-level evidence
| Devices with a numeric GTIN | 10 |
|---|---|
| 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. Rushwood b.v. is registered in the United States but was not found in the Canadian register.