Miracor Medical SA
BE-MF-000001089 · Belgium · Awans
Miracor Medical SA is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 10 |
|---|---|
| Class I | 3 |
| Class IIb | 1 |
Most frequent device types declared: 1.01.4000, 1.02.0001, 1.02.0003, 1.02.0005.
Among these devices, 3 are declared sterile.
Devices declared under this manufacturer
- PiCSO Impulse CSP Cable
- PiCSO Impulse Cart
- PiCSO Impulse Catheter, 1500mm
- PiCSO Impulse Catheter, 1750mm
- PiCSO Impulse Catheter, 2000mm
- PiCSO Impulse Console
- PiCSO Impulse ECG Cable, AHA
- PiCSO Impulse ECG Cable, IEC
- PiCSO Impulse Gas Cartridge
- PiCSO Impulse Power Cord, CH
- PiCSO Impulse Power Cord, EU
- PiCSO Impulse Power Cord, IT
Showing 12 of 14 declared devices.
Catalogue references include 1.01.4000, 1.02.0003, 1.03.0001, 1.03.0003, 1.03.0004, 1.03.0005.
European nomenclature codes declared: Z12059099, C0104020103, C01040180.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| Country of registration | Belgium |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 14 |
|---|---|
| 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. Miracor Medical SA was not found in either the U.S. or the Canadian register.