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Footrest extension

EUDAMED

Class I (EU MDR)

Ref 472.010003Model Accessory to instrument delivery table

by AKRUS GmbH & Co. KG

Identity

Trade Name
Footrest extension EUDAMED
Device Name
IT 1060.i / IT 760.i EUDAMED
Model / Reference
Accessory to instrument delivery table EUDAMED
472.010003 EUDAMED

Identifiers

Primary DI / UDI-DI
04260647940039 EUDAMED
Basic UDI-DI
426064794Zubehoer/ITQQ EUDAMED
Direct Marketing DI
04260647940039 EUDAMED
EMDN Code
Z12129001 OPHTHALMOLOGICAL INSTRUMENT STANDS 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

Footrest extension by AKRUS GmbH & Co. KG — 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

Manufacturer
AKRUS GmbH & Co. KG
EUDAMED SRN
DE-MF-000005262

Sources (1)

  • EUDAMED 8ac38c9e-d441-460b-a7f4-cb47c11d93da 61 fields · synced Jun 19, 2026