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ak 5010 MBS

EUDAMED

Class I (EU MDR)

Ref 277.000000Model Examination chairRef 277.000007

by AKRUS GmbH & Co. KG

Identity

Trade Name
ak 5010 MBS EUDAMED
Device Name
ak 5010 MBS EUDAMED
Model / Reference
Examination chair EUDAMED
277.000000 EUDAMED
277.000007 EUDAMED

Identifiers

Primary DI / UDI-DI
04260647941524 EUDAMED
04260647941555 EUDAMED
Basic UDI-DI
426064794ak5010MBSEU EUDAMED
Direct Marketing DI
04260647941524 EUDAMED
04260647941555 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

ak 5010 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 (4)

  • EUDAMED bcd25da7-afa3-4543-9822-3c9123fb5364 61 fields · synced Jul 17, 2026
  • EUDAMED 11f45027-972f-4009-b120-e052f581689c 61 fields · synced May 19, 2026
  • EUDAMED 82932a27-ed3a-4606-a287-c901159a18db 61 fields · synced Jun 18, 2026
  • EUDAMED f18c6660-2e87-475f-b317-882f00cbcec6 61 fields · synced Jul 17, 2026