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Cheek Retractor

EUDAMED

Class I (EU MDR)

Ref 002

by Anhui Huming Medical Technology Co., Ltd

Identity

Device Name
Cheek Retractor EUDAMED
Model / Reference
002 EUDAMED

Identifiers

Primary DI / UDI-DI
06977449600020 EUDAMED
Basic UDI-DI
6977449600020EY EUDAMED
EMDN Code
V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE 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

Cheek Retractor by Anhui Huming Medical Technology 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-000042851
Authorised Representative
Humiss Beratung GmbH DE-AR-000023447

Sources (1)

  • EUDAMED 8cdb2f16-d3d5-476f-9eed-5d40067f3066 61 fields · synced Jun 18, 2026