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Guide Wire

EUDAMED

Class I (EU MDR)

Ref LG44217Model VBE-2000

by Dragon Crown Medical Co., Ltd.

Identity

Trade Name
Guide Wire EUDAMED
Device Name
V-shape Bichannel Endoscopy System EUDAMED
Model / Reference
VBE-2000 EUDAMED
LG44217 EUDAMED

Identifiers

Primary DI / UDI-DI
06939488527591 EUDAMED
Basic UDI-DI
69394885000GQ6 EUDAMED
EMDN Code
L098003 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY TAPS, 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

Guide Wire 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 c18f84ad-5acf-4c7d-9d0b-0a6f8dbee940 61 fields · synced Oct 6, 2026