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Meridian Medical d.o.o.

Active in EUDAMED

Sloveniafrom SRN EUDAMED FDA SRN SI-MF-000006685 FEI 3029221947

Devices
1
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

EU certificates

3 of 3 in force.

See certificates

Market reach

European Union
EUDAMED actor, 3 certificates
United States
FDA establishment

What Meridian Medical d.o.o. makes

Meridian Medical d.o.o. manufactures the MR Q, a device designed for magnetic resonance imaging (MRI) compatibility and specific diagnostic or interventional use in clinical settings.

The MR Q is classified as a Class IIb medical device and is listed in the EU’s eudamed registry. The company is based in Slovenia.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Mr Q

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:IIb

Company details

EUDAMED SRN
SI-MF-000006685
FDA FEI number
3029221947
EU VAT number
62811649
EUDAMED status
Active
EUDAMED registered name
Meridian Medical d.o.o.
Registered address
8, Plemljeva ulica, 1210, Ljubljana-Šentvid, Slovenia
Phone
+38615007100
PRRC contact
Irena Žnidar(public in EUDAMED)

EUDAMED certificates3

3 certificates3 valid, 0 expiredMDR 3next expiry 22 Mar 2028

EUDAMED certificates (3)

SLOVENIAN INSTITUTE OF QUALITY AND METROLOGY - SIQ 1304 3 certificates

  • MDR-0049 Active Amended

    Quality management system EU MDR

    Issued
    9 Oct 2026
    Expires
    26 Aug 2031
    Reason
    Other
  • MDR-0015 Active Amended

    Quality management system EU MDR

    Issued
    3 Oct 2025
    Expires
    8 Aug 2029
    Reason
    Other
  • MDR-001 Active Amended

    Quality management system EU MDR

    Issued
    10 Jun 2025
    Expires
    22 Mar 2028
    Reason
    Mnf data change

FDA establishments1

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

  • Meridian Medical d.o.o. US

Frequently asked questions

How many devices does Meridian Medical d.o.o. have in the registry?

The registry currently lists 1 device for Meridian Medical d.o.o.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Meridian Medical d.o.o.'s devices?

Among its 1 most recently registered device, Meridian Medical d.o.o. has devices listed in EUDAMED (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Meridian Medical d.o.o.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Meridian Medical d.o.o.'s devices are Class IIb. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for Meridian Medical d.o.o.?

EUDAMED lists 3 certificates for Meridian Medical d.o.o. (quality management system) under MDR. The most recent was issued on 9 Oct 2026.

What are the newest devices from Meridian Medical d.o.o. in the registry?

The most recently registered devices listed for Meridian Medical d.o.o. include MR Q.

Which FDA establishments are linked to Meridian Medical d.o.o.?

1 FDA establishment is linked to Meridian Medical d.o.o. in the registry; they are listed on the company page.

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