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2.8v Professional/Practitioner Diagnostic Set

EUDAMED

Class I (EU MDR)

Ref 1729-P-1046

by Keeler Ltd

Identity

Trade Name
2.8V PROFESSIONAL/PRACTITIONER DIAGNOSTIC SET EUDAMED
Device Name
Ophthalmic/otologic diagnostic set EUDAMED
Model / Reference
1729-P-1046 EUDAMED

Identifiers

Primary DI / UDI-DI
05055272716741 EUDAMED
Basic UDI-DI
5055272745084XR EUDAMED
Direct Marketing DI
05055272716741 EUDAMED
EMDN Code
Z12120199 OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHER 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

2.8v Professional/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

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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 1d060a3a-370a-4cf7-a864-d7d02caadb08 61 fields · synced Jun 18, 2026