SyntheticMR AB

Sweden SE-MF-000003513 Last updated 23 Oct 2026

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Devices: 3
Registries: EUDAMEDGUDIDFDA
FDA recalls: 0

Catalogue3

SyMRI 15 Ref 0007

Class IIa EUDAMEDFDA UDI Active
cNeuro cMRI Ref 0

Class IIa EUDAMED Active
SyMRI 12 Ref 0004

Class IIa EUDAMED Active

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

Intertek Medical Notified Body AB 2862 1 certificate

28620110677-01 Supplemented

Quality management system EU MDR

Issued
8 Jun 2026

Expires
30 Sep 2027

Reason
Other

Notified bodies

Intertek Medical Notified Body AB 2862

Information

Country: Sweden
Address: 11, Storgatan, Linköping, Sweden
Website: www.syntheticmr.com
Email: [email protected]
Phone: +46 (0) 13 101 650
PRRC contact: Lisa Warnroth
EUDAMED SRN: SE-MF-000003513
FDA FEI number: 3014111222