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Flat Panel Detector

by Shanghai PZ Medical Technology Co., Ltd.

Ref Ref_Encoding rules, Ref_Encoding rules for serial numbersModel 2925A, 3543Z, 3025ZF, 6543Z, 2121Z, 4343ZF, 3543ZF, 4343Z, 4386Z, 3025Z, 3030Z

Flat Panel Detector (Ref_Encoding rules) is a Class IIa device made by Shanghai PZ Medical Technology Co., Ltd., registered in EUDAMED on 31 Jan 2024 (Basic UDI-DI 6976059772925AA4), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6976059772925AA4 Basic UDI-DI Date31 Jan 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
2925A, Ref_Encoding rules, 3543Z, 3025ZF, Ref_Encoding rules for serial numbers, 6543Z, 2121Z, 4343ZF, 3543ZF, 4343Z, 4386Z, 3025Z, 3030Z
Primary DI / UDI-DI
06976059770208, 06976059770048, 06976059770031, 06976059770161, 06976059770178, 06976059770062, 06976059770055, 06976059770147, 06976059770017, 06976059770123, 06976059770130
Basic UDI-DI
6976059772925AA4, 6976059773543ZB9, 6976059773025ZF75, 6976059776543ZCA, 6976059772121Z9J, 6976059774343ZF8P, 6976059773543ZF8Y, 6976059774343ZB6, 6976059774386ZC3, 6976059773025ZA2, 6976059773030Z9Q
Direct marketing DI
06976059770048
06976059770031
06976059770161
06976059770062
06976059770055
06976059770147
06976059770123
EMDN code
Z11079099 Various x–ray film imaging support instruments - other
Device class
Class IIa
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000035699
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Similar devices in this category

Other devices filed under VARIOUS SUPPORTING INSTRUMENTS FOR X–RAY FILM IMAGING.

Properties

  • Reusable NoEUDAMEDYesEUDAMED
  • Administering medicine YesEUDAMEDNoEUDAMED
  • Measuring function
Other properties (11, all answered No)