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10HQ701G-B

by LG Electronics Inc.

Ref 10HQ701G-BP

Active European Union

CE MDR

Valid until

Not listed

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

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

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8806098DETECTOR-AWSW3 Basic UDI-DI Date12 Sep 2023RegisteredStatusActive

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

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Flat Panel Digital X-ray Detector
Model / Reference
10HQ701G-BP
Primary DI / UDI-DI
08806091878182, 08806091876980, 08806091876942
Basic UDI-DI
8806098DETECTOR-AWSW3
EMDN Code
Z11030580 Radiology instruments - hardware accessories
Device Class
Class IIb
EU market of registration
Germany
Hungary
Northern Ireland

Manufacturer details

EUDAMED SRN
KR-MF-000001897
Authorised representative
LG Electronics Deutchland GmbH DE-AR-000044729

Other devices from LG Electronics Inc.

See all devices from LG Electronics Inc. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No