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Rxrcspled

EUDAMED

Class I (EU MDR)

Ref 109821Model RXRCSPLED

by Neitz Instruments Co., Ltd.

Identity

Trade Name
RXRCSPLED EUDAMED
Device Name
Retinoscope EUDAMED
Model / Reference
RXRCSPLED EUDAMED
109821 EUDAMED

Identifiers

Primary DI / UDI-DI
04571328653446 EUDAMED
Basic UDI-DI
45713286534463G EUDAMED
EMDN Code
Z12120118 RETINOSCOPES EUDAMED

Classification

Device Class
Class I 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Rxrcspled by Neitz Instruments Co., Ltd. — Class I — 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

EUDAMED SRN
JP-MF-000048706
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 7e069ff4-9a53-4d0e-be1c-62e1ac1ef5c3 61 fields · synced Jul 29, 2026