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0.7/1.2JG326D-265

by Shimadzu Corporation

Ref 582-24825-42

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04540217060788 Basic UDI-DI 04540217060788UDI-DIDate10 Mar 2023RegisteredStatusActive
United StatesGUDID listing GUDID Number04540217060788 UDI-DI Date23 Jul 2019ListedStatusListed 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  • Withdrawn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
0.7/1.2JG326D-265 EUDAMED
0.7/1.2JG326 D-265 GUDID
Generic Name
X-ray tube housing assembly, diagnostic
Device Name
X-ray tube assembly 0.7/1.2JG326D-265
Model / Reference
582-24825-42
Primary DI / UDI-DI
04540217060788
Basic UDI-DI
B-04540217060788
FDA Product Code
ITY
EMDN Code
Z11039012 X-ray tube assembly
GMDN Term
X-ray tube housing assembly, diagnostic
Device Class
Class IIb EUDAMED
Class I GUDID
Regulation Number
892.1760
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIb
GUDID
Class I

Manufacturer details

EUDAMED SRN
JP-MF-000025145
Authorised representative
Shimadzu Europa GmbH DE-AR-000013563

Other devices from Shimadzu Corporation

See all devices from Shimadzu Corporation →

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

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
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No