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Redsense Medical AB

Sweden SE-MF-000005240 Last updated 25 Oct 2026

Devices
9
Registries
EUDAMEDGUDIDFDA 510(k)FDA
FDA recalls
0

Catalogue9

About

Redsense cares about your safety Let Redsense keep an eye on your access Our products

From the manufacturer's own website. Source

What Redsense Medical AB makes

Redsense Medical AB manufactures medical devices for monitoring and alarm systems in vascular access applications, including clamp systems, sensor patches for venous and catheter use, and standalone alarm units with integrated sensors. Their portfolio also includes home-use alarm systems and European Union-compliant chargers for these devices.

The company’s products are classified under EU Medical Device Regulations as Class I and Class II, with some devices listed in the EUDAMED registry and others subject to FDA 510(k) clearance in the United States. The manufacturer is based in Sweden.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
Sweden(from SRN)
Address
36, Storgatan, Halmstad, Sweden
Phone
+46 35 1060 30
PRRC contact
Ann-Marie Eriksson
EUDAMED SRN
SE-MF-000005240
FDA FEI number
3006948863