← Back to catalogue

Laryngoscope

EUDAMED

Class I (EU MDR)

Ref H901ABModel H707AB、H706AB、H901AB、H906AB

by Wuzhou Aokace Technology Co., Ltd.

Identity

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

Identifiers

Primary DI / UDI-DI
06975465800400 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED a4db1200-c4b4-4d5c-9a06-ae0a29efc5a3 61 fields · synced Jun 19, 2026