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Laryngoscope

EUDAMED

Class I (EU MDR)

Ref H706ABModel H707AB、H706AB、H901AB、H906ABRef H906AB

by Wuzhou Aokace Technology Co., Ltd.

Identity

Trade Name
Laryngoscope EUDAMED
Device Name
Laryngoscope EUDAMED
Model / Reference
H707AB、H706AB、H901AB、H906AB EUDAMED
H706AB EUDAMED
H906AB EUDAMED

Identifiers

Primary DI / UDI-DI
06975465800394 EUDAMED
06975465800417 EUDAMED
Basic UDI-DI
697546580LHABQW EUDAMED
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Laryngoscope blade, reusable

Laryngoscope by Wuzhou Aokace Technology Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000027213
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED 4d3a15f0-23eb-49a6-951d-22d521714568 61 fields · synced Sep 18, 2026
  • EUDAMED 1830e467-632a-40ac-831d-c54c1f44f1b9 61 fields · synced May 18, 2026