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Video Colonoscope

EUDAMED

Class IIa (EU MDR)

Ref /Model CVE-2900HT/CVE-2900HL/CVE-2900HI/CVE-2900HS/CVE-3000HT/CVE-3000HL/CVE-3000HI/CVE-3000HTW/CVE-3000HLW/CVE-3000HIW/CVE-3500HT/CVE-3500HL/CVE-3500HI/CVE-3500HS

by HUGER Medical Instrument Co., Ltd.

Identity

Device Name
Video Colonoscope EUDAMED
Model / Reference
CVE-2900HT/CVE-2900HL/CVE-2900HI/CVE-2900HS/CVE-3000HT/CVE-3000HL/CVE-3000HI/CVE-3000HTW/CVE-3000HLW/CVE-3000HIW/CVE-3500HT/CVE-3500HL/CVE-3500HI/CVE-3500HS EUDAMED
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06953393165037 EUDAMED
Basic UDI-DI
69533931COFS EUDAMED
EMDN Code
Z12020606 VIDEO COLONOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Video Colonoscope by HUGER Medical Instrument Co., Ltd. — Class IIa — 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

Manufacturer
HUGER Medical Instrument Co., Ltd.
EUDAMED SRN
CN-MF-000001128
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 689fee3e-bb45-4378-99c5-9f251b07db62 61 fields · synced Jun 19, 2026