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Gonioscope Gs-1

EUDAMED

Class IIa (EU MDR)

Ref B01E007Model GS-1

by NIDEK.CO.Ltd.,

Identity

Trade Name
GONIOSCOPE GS-1 EUDAMED
Model / Reference
GS-1 EUDAMED
B01E007 EUDAMED

Identifiers

Primary DI / UDI-DI
04987669101582 EUDAMED
Basic UDI-DI
4987669212G7 EUDAMED
EMDN Code
Z12120114 OPHTHALMOSCOPES 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Gonioscope Gs-1 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 12f64ce8-80f2-4ef5-9503-6f8319a1878d 61 fields · synced Jul 31, 2026