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D-Kat (r-Type) With Certificate

EUDAMED

Class IIa (EU MDR)

Ref 2414-P-2042C

by Keeler Ltd

Identity

Trade Name
D-KAT (R-TYPE) WITH CERTIFICATE EUDAMED
Device Name
D-KAT (R-TYPE) WITH CERTIFICATE EUDAMED
Model / Reference
2414-P-2042C EUDAMED

Identifiers

Primary DI / UDI-DI
05055272714860 EUDAMED
Basic UDI-DI
B-05055272714860 EUDAMED
EMDN Code
Z12120122 TONOMETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

D-Kat (r-Type) With Certificate by Keeler Ltd — Class IIa — 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 fdcea42d-187e-4814-8852-2c8ddf2560cc 61 fields · synced Jul 20, 2026