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Mim 7.5

by Mim Software Inc.

Ref 6003987Model MIM Maestro, MIM Encore, MIMcardiac, MIMneuro, MIM Sureplan Liver Y90, MIM SurePlan MRT, MIM Symphony, MIM SPECTRA Quant

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00850009343352 Basic UDI-DI 00850009343352UDI-DIDate10 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00850009343352 UDI-DI Date30 Jan 2026ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Mim
Generic Name
Radiological PACS-dedicated management software
Model / Reference
MIM Maestro EUDAMED
MIM Encore EUDAMED
MIMcardiac EUDAMED
MIMneuro EUDAMED
MIM Sureplan Liver Y90 EUDAMED
MIM SurePlan MRT EUDAMED
MIM Symphony EUDAMED
MIM SPECTRA Quant EUDAMED
6003987 EUDAMED
7.5 GUDID
Primary DI / UDI-DI
00850009343352
Basic UDI-DI
B-00850009343352
FDA Product Code
LLZ, QTZ
EMDN Code
Z110603 Picture archiving and communication systems
GMDN Term
Radiological PACS-dedicated management software
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
892.2050
Special Device Type
-1192
EU market of registration
Finland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Other devices from Mim Software Inc.

See all devices from Mim Software Inc. →

Properties

  • Measuring Function
  • Prescription Use
  • Lot / Batch Number

Other properties (19)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No