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Video Laryngoscope Blade

EUDAMED

Class I (EU MDR)

Ref HT3Model HT2,HT3,HT4,HT M3,HT M4,HT P2,HT ML0

by Shenzhen HugeMed Medical Technical Development Co., Ltd.

Identity

Device Name
Video Laryngoscope Blade EUDAMED
Model / Reference
HT2,HT3,HT4,HT M3,HT M4,HT P2,HT ML0 EUDAMED
HT3 EUDAMED

Identifiers

Primary DI / UDI-DI
06970462541325 EUDAMED
Basic UDI-DI
69704625421077W EUDAMED
Direct Marketing DI
06970462541325 EUDAMED
EMDN Code
Z12021004 VIDEO LARYNGOSCOPES EUDAMED

Classification

Device Class
Class I 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

Video Laryngoscope Blade by Shenzhen HugeMed Medical Technical Development Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000010895
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 73db5e38-d920-467c-865f-3bb02d40d5ef 61 fields · synced Jun 18, 2026