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31hn713d

EUDAMEDFDA 510(k)

Class IIa (EU MDR)

Ref 31HN713D-M510(k) K201777

by LG Electronics Inc.

Identity

Trade Name
31HN713D EUDAMED
Device Name
MEDICAL MONITOR EUDAMED
Model / Reference
31HN713D-M EUDAMED

Identifiers

Primary DI / UDI-DI
08806096367865 EUDAMED
Basic UDI-DI
8806098MNT-2MAMMO46 EUDAMED
EMDN Code
Z11900801 BIOIMAGING DIAGNOSTIC REPORT VIEWING MONITORS 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

31hn713d 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
FDA Applicant
Lg Electronics.Inc
Authorised Representative
LG Electronics Deutchland GmbH DE-AR-000044729

Sources (2)

  • EUDAMED 83ff58d5-ed94-47da-80fb-3308566926db 85 fields · synced Jun 18, 2026
  • FDA 510(k) K201777 1 fields · synced May 18, 2026