Redsense Medical AB
SE-MF-000005240 · Sweden · Halmstad
Redsense Medical AB is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: Redsense Alarm fiber optic extension (FOE), Redsense Alarm system EU charger, Redsense Alarm unit with FOE, IFU, charger EU, Redsense Catheter Sensor Patch, Redsense Clamp System.
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- Redsense Alarm system EU charger
- Redsense Alarm unit with FOE, IFU, charger EU
- Redsense Catheter Sensor Patch
- Redsense Clamp System
- Redsense FOE
- Redsense Venous Sensor Patch
Catalogue references include RA-1-RA201-A, RB-1-RB201, RC-1-RC201-A, RE-1-RE201, RL-1-RL201-S, RS-1-RS201-S.
European nomenclature codes declared: F9099.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | REDSENSE MEDICAL AB (SE) · FDA 3006948863 |
| Devices in EUDAMED | 7 |
| Country of registration | Sweden |
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | REDSENSE MEDICAL AB |
North American profile: Both markets. Redsense Medical AB is registered in both the United States and Canada.