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K-Led + Double Charger + 1 Battery

EUDAMED

Class I (EU MDR)

Ref 2004-P-1008

by Keeler Ltd

Identity

Trade Name
K-LED + DOUBLE CHARGER + 1 BATTERY EUDAMED
Device Name
K-LED II EUDAMED
Model / Reference
2004-P-1008 EUDAMED

Identifiers

Primary DI / UDI-DI
05055272711258 EUDAMED
Basic UDI-DI
50552727KLEDMC EUDAMED
Direct Marketing DI
05055272711258 EUDAMED
EMDN Code
Z12010702 MOBILE SCIALYTIC LAMPS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Bulgaria 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

K-Led + Double Charger + 1 Battery by Keeler 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
Keeler Ltd
EUDAMED SRN
GB-MF-000009031
Authorised Representative
Keeler Europe Distribution, S.L. ES-AR-000001559

Sources (1)

  • EUDAMED 32a36144-d564-44f1-9fe5-5f42a7020abf 61 fields · synced Jul 19, 2026