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IX73

by Evident Corporation

Ref N6792000

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

CE IVDR

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number458264313IX73DG Basic UDI-DI 04582754071520UDI-DIDate28 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04582754071520 UDI-DI Date31 Oct 2025ListedStatusListed 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  • Withdrawn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/IVDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
IX73 2PORT Frame
Generic Name
Inverted-stage light microscope
Device Name
IX73
Model / Reference
N6792000 EUDAMED
IX73P2F-1-2 GUDID
Primary DI / UDI-DI
04582754071520
Basic UDI-DI
458264313IX73DG
FDA Product Code
MTX
EMDN Code
W0202050303 Optical laboratory microscopes
GMDN Term
Inverted-stage light microscope
Device Class
Class A EUDAMED
Class I GUDID
Regulation Number
884.6190
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
N6792000
GUDID
IX73P2F-1-2
Device ClassEUDAMED
Class A
GUDID
Class I

Manufacturer details

EUDAMED SRN
JP-MF-000027470
Authorised representative
Evident Europe GmbH DE-AR-000025360

Other devices from Evident Corporation

See all devices from Evident Corporation →

Properties

  • Surgical Instrument
  • Premarket Exempt
  • Serial Number

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • New Device: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No