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Wypklene-S

EUDAMED

Class I (EU MDR)

Ref WYPKLENE-SModel B-EGT100200-P

by GBUK Group

Identity

Model / Reference
B-EGT100200-P EUDAMED
WYPKLENE-S EUDAMED

Identifiers

Primary DI / UDI-DI
05060405745963 EUDAMED
Basic UDI-DI
506040574SlideSheetsVN EUDAMED
Direct Marketing DI
05060405745963 EUDAMED
EMDN Code
V0899 MEDICAL SUPPORT EQUIPMENT - OTHER 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

Wypklene-S by GBUK Group — 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

Manufacturer
GBUK Group
EUDAMED SRN
GB-MF-000002238
Authorised Representative
Qualrep Services B.V. NL-AR-000000537

Sources (1)

  • EUDAMED d66362e8-6064-49e6-b6c7-0d911df51944 61 fields · synced Aug 3, 2026