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Tonoclear

EUDAMED

Class I (EU MDR)

Ref 2414-P-7045

by Keeler Ltd

Identity

Trade Name
TONOCLEAR EUDAMED
Device Name
TONOCLEAR EUDAMED
Model / Reference
2414-P-7045 EUDAMED

Identifiers

Primary DI / UDI-DI
05055272720205 EUDAMED
Basic UDI-DI
B-05055272720205 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

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Tonoclear by Keeler Ltd — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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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 e670e687-397c-4b14-96eb-d9b86c79b74f 61 fields · synced Jun 19, 2026