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Auto Ref/Kerato/Tono/Pachymeter Tonoref Iii

EUDAMED

Class IIa (EU MDR)

Ref B01E005Model TONOREF III

by NIDEK.CO.Ltd.,

Identity

Trade Name
AUTO REF/KERATO/TONO/PACHYMETER TONOREF III EUDAMED
Model / Reference
TONOREF III EUDAMED
B01E005 EUDAMED

Identifiers

Primary DI / UDI-DI
04987669101674 EUDAMED
Basic UDI-DI
4987669207GE EUDAMED
EMDN Code
Z12120113,Z12120122,Z12120180 EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Auto Ref/Kerato/Tono/Pachymeter Tonoref Iii by Nidek Co., Ltd. — 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
NIDEK.CO.Ltd.,
EUDAMED SRN
JP-MF-000040151
Authorised Representative
NIDEK SA FR-AR-000000341

Sources (1)

  • EUDAMED 27e16656-76f3-4274-9fbd-07e662b6be04 61 fields · synced Jun 19, 2026