FEops NV

Belgium BE-MF-000001008 Last updated 23 Oct 2026

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Devices: 3
Registries: EUDAMEDGUDIDFDA
FDA recalls: 0

Catalogue3

FEops HEARTguide Ref 05430002070148

Class IIa EUDAMEDFDA UDI Active
FEops HEARTguide Ref 05430002070124

Class IIa EUDAMEDFDA UDI Active
FEops HEARTguide Ref 05430002070131

Class IIa EUDAMEDFDA UDI Active

EUDAMED certificates2

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

Notified body 1912 2 certificates

24M00068CRT01 Reissued

Quality management system EU MDR

Issued
28 Sep 2024

Expires
28 Sep 2029
20M00129CRT04 Expired

Quality management system EU MDR

Issued
28 Sep 2021

Expires
28 Sep 2024

Notified bodies

Notified body 1912

FDA establishments1

Registered with the FDA under this company group, matched by name.

FEops US

Information

Country: Belgium
Address: 122, Technologiepark-Zwijnaarde, Gent, Belgium
Website: www.feops.com
Email: [email protected]
Phone: +32 492 50 19 51
PRRC contact: Franky Dubois
EUDAMED SRN: BE-MF-000001008
FDA FEI number: 3020703662