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Kemagel® Conductive

EUDAMED

Class I (EU MDR)

Ref GELCON5000

by Pharmaplast

Identity

Trade Name
Kemagel® Conductive EUDAMED
Device Name
Kemagel conductive EUDAMED
Model / Reference
GELCON5000 EUDAMED

Identifiers

Primary DI / UDI-DI
06222023895379 EUDAMED
Basic UDI-DI
62220238KemagelCXV EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland 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

Category: Device sterilization/disinfection container, reusable

Kemagel® Conductive by Pharmaplast — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Pharmaplast
EUDAMED SRN
EG-MF-000004501
Authorised Representative
E C REP LIMITED IE-AR-000003995

Sources (1)

  • EUDAMED dd549556-92b8-47c1-b7d6-b51baae5d119 61 fields · synced Jun 19, 2026