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lmuderm Emollient

EUDAMED

Class I (EU MDR)

Ref IMU500EM

by Clinisupplies Ltd

Identity

Trade Name
lmuderm Emollient EUDAMED
Device Name
WOUND CARE EUDAMED
Model / Reference
IMU500EM EUDAMED

Identifiers

Primary DI / UDI-DI
05036100015892 EUDAMED
Basic UDI-DI
50361000W00185 EUDAMED
Direct Marketing DI
05036100015892 EUDAMED
EMDN Code
M9002 PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS) 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

lmuderm Emollient by Clinisupplies 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

Manufacturer
Clinisupplies Ltd
EUDAMED SRN
GB-MF-000023783
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 056c156b-d706-4d3f-907a-a9c7b7b3c870 61 fields · synced Jul 12, 2026