Ferrosan Medical Devices A/S
DK-MF-000002856 · Denmark · Søborg
Ferrosan Medical Devices A/S is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class I | 6 |
|---|
Most frequent device types declared: MS0002, MS0004, MS0005, MS0006, MS0007.
Among these devices, 6 are declared sterile.
Devices declared under this manufacturer
- SPONGOSTAN™
Catalogue references include MS0002, MS0004, MS0005, MS0006, MS0007, MS0008.
European nomenclature codes declared: M040503, M040599.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | FERROSAN MEDICAL DEVICES A/S (DK) · FDA 3008478369 |
| Devices in EUDAMED | 6 |
| Country of registration | Denmark |
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | FERROSAN MEDICAL DEVICES A/S |
What it holds in Canada
| Licences on record | 2 |
|---|---|
| Currently active | 0 |
| Class 4 devices | 2 |
| First licensed | 1999-09-28 |
Licence types: Device Family (1), Device Group Family (1).
Licensed under: ABSORBABLE GELATIN SPONGE, SURGIFLO HEMOSTATIC MATRIX.
North American profile: Both markets. Ferrosan Medical Devices A/S is registered in both the United States and Canada.