MRC Holland B.V.
NL-MF-000000437 · Netherlands · Amsterdam
MRC Holland B.V. is registered in the European database on medical devices as a manufacturer, with 142 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: B1, B2, B3, B4, C1.
Devices declared under this manufacturer
- SALSA MLPA Probemix P002 BRCA1
- SALSA MLPA Probemix P017 MEN1
- SALSA MLPA Probemix P033 CMT1
- SALSA MLPA Probemix P050 CAH
- SALSA MLPA Probemix P060 SMA Carrier
- SALSA MLPA Probemix P093 HHT/HPAH
- SALSA MLPA Probemix P138 SLC2A1-STXBP1
- SALSA MLPA Probemix P189 CDKL5-FOXG1
- SALSA MLPA Probemix P213 HSP mix-2
- SALSA MLPA Probemix P226 SDH
- SALSA MLPA Probemix P250 DiGeorge
- SALSA MLPA Probemix P260 PALB2-RAD50-RAD51C-RAD51D
Showing 12 of 142 declared devices.
Catalogue references include P017-050R, P033-100R, P060-100R, P093-100R, P138-050R, P213-025R.
European nomenclature codes declared: W0106010199, W0106010199,W01060299, W0106010399, W0106010108,W010699, W0106010401, W0106010109,W0106010111,W0106010199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 142 |
| 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 | 142 |
|---|---|
| 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. MRC Holland B.V. was not found in either the U.S. or the Canadian register.