← Back to catalogue

3.6v Practitioner Diagnostic Set

EUDAMED

Class I (EU MDR)

Ref 1964-P-2002

by Keeler Ltd

Identity

Trade Name
3.6V PRACTITIONER DIAGNOSTIC SET EUDAMED
Device Name
Ophthalmic/otologic diagnostic set EUDAMED
Model / Reference
1964-P-2002 EUDAMED

Identifiers

Primary DI / UDI-DI
05055272703031 EUDAMED
Basic UDI-DI
5055272745084XR EUDAMED
Direct Marketing DI
05055272703031 EUDAMED
EMDN Code
Z12120199 OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHER 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

3.6v Practitioner Diagnostic Set 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 3992d5cf-7f81-4983-8ce1-6531e8eea78b 61 fields · synced Jun 19, 2026