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Full Auto Ref-Keratometer RK-F3m

EUDAMED

Class IIa (EU MDR)

Ref RB-A20A-B009Model Full Auto Ref-Keratometer

by Canon Inc.

Identity

Trade Name
Full Auto Ref-Keratometer RK-F3m EUDAMED
Device Name
RK-F3m EUDAMED
Model / Reference
Full Auto Ref-Keratometer EUDAMED
RB-A20A-B009 EUDAMED

Identifiers

Primary DI / UDI-DI
04549292214802 EUDAMED
Basic UDI-DI
4549292rk01ET EUDAMED
EMDN Code
Z12120113 OPHTHALMOMETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands 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

Full Auto Ref-Keratometer RK-F3m by Canon Inc. — Class IIa — 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
Canon Inc.
EUDAMED SRN
JP-MF-000013254
Authorised Representative
Canon Medical Systems Europe B.V. NL-AR-000010531

Sources (1)

  • EUDAMED 7e815c0c-2614-410f-a035-39bba1d55aa2 61 fields · synced Jul 26, 2026