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Oakmed

EUDAMED

Class I (EU MDR)

Ref LPSCA28-4115KV

by Oakmed Ltd

Identity

Trade Name
Oakmed EUDAMED
Device Name
Oakmed Stoma Care and Wound Care products EUDAMED
Model / Reference
LPSCA28-4115KV EUDAMED

Identifiers

Primary DI / UDI-DI
05060577755807 EUDAMED
Basic UDI-DI
506057775StomaCareR5 EUDAMED
EMDN Code
A1001010202,A1001020202,A1001030202 EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
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

Oakmed by Oakmed 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
Oakmed Ltd
EUDAMED SRN
UK-MF-000051482
Authorised Representative
Specculo Limited MT-AR-000034988

Sources (1)

  • EUDAMED e7f72d19-6712-4464-b641-fcaedeee2e21 61 fields · synced Jun 18, 2026