← Back to catalogue

2.8v Practitioner Oto

EUDAMED

Class I (EU MDR)

Ref 1513-P-1062

by Keeler Ltd

Identity

Trade Name
2.8V PRACTITIONER OTO EUDAMED
Device Name
Keeler Otoscopes EUDAMED
Model / Reference
1513-P-1062 EUDAMED

Identifiers

Primary DI / UDI-DI
05055272701990 EUDAMED
Basic UDI-DI
50552727OTOSCOPESVJ EUDAMED
Direct Marketing DI
05055272701990 EUDAMED
EMDN Code
Z12149006 DIRECT OUTPATIENT OTOSCOPES 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

2.8v Practitioner Oto 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Keeler Ltd
EUDAMED SRN
GB-MF-000009031
Authorised Representative
Keeler Europe Distribution, S.L. ES-AR-000001559

Sources (1)

  • EUDAMED 88d42475-7a44-417a-9a82-7cda06a83a3d 61 fields · synced Jun 20, 2026