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17hq701g-B

EUDAMEDFDA 510(k)

Class IIa (EU MDR)

Ref 17HQ701G-BA

by LG Electronics Inc.

Identity

Trade Name
17HQ701G-B EUDAMED
Device Name
Flat Panel Digital X-ray Detector EUDAMED
Model / Reference
17HQ701G-BA EUDAMED

Identifiers

Primary DI / UDI-DI
08806091932211 EUDAMED
Basic UDI-DI
8806098DETECTORCK EUDAMED
EMDN Code
Z11030580 RADIOLOGY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

17hq701g-B by LG Electronics Inc. — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

Manufacturer
LG Electronics Inc.
EUDAMED SRN
KR-MF-000001897
Authorised Representative
LG Electronics Deutchland GmbH DE-AR-000044729

Sources (2)

  • EUDAMED dd6edaab-8cef-4308-81c6-1dc02a51507a 61 fields · synced Jun 18, 2026
  • FDA 510(k) K221434 1 fields · synced May 18, 2026