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Dilation Tube

EUDAMED

Class I (EU MDR)

Ref L0925Model VBE-2000

by Dragon Crown Medical Co., Ltd.

Identity

Trade Name
Dilation Tube EUDAMED
Device Name
V-shape Bichannel Endoscopy System EUDAMED
Model / Reference
VBE-2000 EUDAMED
L0925 EUDAMED

Identifiers

Primary DI / UDI-DI
06939488527638 EUDAMED
Basic UDI-DI
69394885000GQ6 EUDAMED
EMDN Code
L0925 ORTHOPAEDIC SURGERY DILATORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye 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

Dilation Tube by Dragon Crown Medical 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-000032712
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED d6b8b090-5142-4d9a-a39a-2ec2eef95d2a 61 fields · synced Jul 28, 2026