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Led Practitioner Otoscope Kit, Aa Battery

EUDAMED

Class I (EU MDR)

Ref 1519-P-1004

by Keeler Ltd

Identity

Trade Name
LED PRACTITIONER OTOSCOPE KIT, AA BATTERY EUDAMED
Device Name
Keeler Otoscopes EUDAMED
Model / Reference
1519-P-1004 EUDAMED

Identifiers

Primary DI / UDI-DI
05055272721462 EUDAMED
Basic UDI-DI
50552727OTOSCOPESVJ EUDAMED
Direct Marketing DI
05055272721462 EUDAMED
EMDN Code
Z12149006 DIRECT OUTPATIENT OTOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Led Practitioner Otoscope Kit, Aa 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 8a29768b-d6ba-470c-88dc-8fa3e99389f0 61 fields · synced Jun 19, 2026