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Vibid

EUDAMED

Class IIb (EU MDR)

Ref WS-COB30NU-1

by Woosung Medi-Filtech

Identity

Trade Name
VIBID EUDAMED
Device Name
VIBID EUDAMED
Model / Reference
WS-COB30NU-1 EUDAMED

Identifiers

Primary DI / UDI-DI
08800017600376 EUDAMED
Basic UDI-DI
B-08800017600376 EUDAMED
EMDN Code
N02010102 PERIDURAL / EPIDURAL CATHETERS FOR CONTINUOUS ANALGESIA AND KITS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Vibid by Woosung Medi-Filtech — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
KR-MF-000004529
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (1)

  • EUDAMED 94d4da0a-d6ee-4a32-a9a2-b81ecd24e8ba 61 fields · synced Jun 18, 2026