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Additive Back support (viscoel.) MBS

EUDAMED

Class I (EU MDR)

Ref 277.032020Model ak 5010 MBS

by AKRUS GmbH & Co. KG

Identity

Trade Name
Additive Back support (viscoel.) MBS EUDAMED
Device Name
Accessories for ak 5010 MBS EUDAMED
Model / Reference
ak 5010 MBS EUDAMED
277.032020 EUDAMED

Identifiers

Primary DI / UDI-DI
04260647942057 EUDAMED
Basic UDI-DI
426064794Zubehoer/MBSE5 EUDAMED
Direct Marketing DI
04260647942057 EUDAMED
EMDN Code
Z12011201 OPERATING CHAIRS 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

Additive Back support (viscoel.) MBS 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 (2)

  • EUDAMED 04e7f3b7-0e7e-4a15-a922-aa3ca82742b0 61 fields · synced Jun 20, 2026
  • EUDAMED 2ba109d5-91dd-4f9d-9bc1-9f62d819f3f8 61 fields · synced Jun 20, 2026