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Quibim S.L.

Active in EUDAMED

Spainfrom SRN EUDAMED FDA SRN ES-MF-000000668 FEI 3025343020

Devices
9
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

EU certificates

1 of 1 in force.

See certificates

Market reach

European Union
EUDAMED actor, 1 certificate
United States
FDA FEI

Catalogue9

Newest first, rows 1-9 of 9

  • QP-Viewer® Ref 1.0

    Class IIa
    Active CE MDR EUDAMED IIa
  • QP-Breast® Ref 1.0

    Class IIb
    Active CE MDR EUDAMED IIb
  • QP-Prostate® Ref 3.0

    Class IIb
    Active CE MDR EUDAMED IIb
  • QUIBIM Precision Prostate (qp-Prostate) Ref K203582

    Class II
    Active 510(k) 510(k) II
  • QP-Prostate® CAD Ref K242683

    Class II
    Active CE MDR 510(k) 510(k) II
  • QP-Liver® Ref 1.1

    Class IIa
    Active CE MDR EUDAMED IIa
  • QP-Prostate® Ref 2.3

    Class IIb
    Active CE MDR EUDAMED IIb
  • QP-Brain® Ref 1.0

    Class IIa
    Active CE MDR 510(k) EUDAMEDGUDID IIa
  • QP-Prostate® Ref 2.4

    Class IIb
    Active CE MDR EUDAMED IIb

Company details

EUDAMED SRN
ES-MF-000000668
FDA FEI number
3025343020
EU VAT number
ES B98481658
EUDAMED status
Active
EUDAMED registered name
QUIBIM S.L.
EUDAMED abbreviated name
QUIBIM
Registered address
30, Avenida Aragón, 30, 13th floor, Office J, 46021, Valencia (Spain), 46021, Valencia, Spain
Phone
+34 961243225
PRRC contact
Erick Murillo Mateo(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 11 Oct 2027

EUDAMED certificates (1)

Notified body 2797 1 certificate

  • MDR 752989 Supplemented

    Quality management system EU MDR

    Issued
    29 Jul 2026
    Expires
    11 Oct 2027
    Reason
    Add device or group

Frequently asked questions

How many devices does QUIBIM S.L. have in the registry?

The registry currently lists 9 devices for QUIBIM S.L.. Devices recorded under merged duplicate company entries are counted once.

Which registries list QUIBIM S.L.'s devices?

Among its 9 most recently registered devices, QUIBIM S.L. has devices listed in EUDAMED (7 devices), FDA 510(k) (2 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.

What risk classes do QUIBIM S.L.'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for QUIBIM S.L.'s devices are Class IIa, Class IIb and Class II. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for QUIBIM S.L.?

EUDAMED lists 1 certificate for QUIBIM S.L. (quality management system) under MDR. The most recent was issued on 2026-07-29.

What are the newest devices from QUIBIM S.L. in the registry?

The most recently registered devices listed for QUIBIM S.L. include QP-Viewer®, QP-Breast®, QP-Prostate® and QUIBIM Precision Prostate (qp-Prostate).

Generated automatically from registry data and not verified by a human reviewer.