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Aesculap

EUDAMED

Class IIa (EU MDR)

Ref GE326SU

by Aesculap AG

Identity

Trade Name
Aesculap EUDAMED
Device Name
PS-Tools saw blade f competitor coupling EUDAMED
Model / Reference
GE326SU EUDAMED

Identifiers

Primary DI / UDI-DI
04046963836078 EUDAMED
Basic UDI-DI
40392390000026773E EUDAMED
EMDN Code
Z12130502 ORTHOPAEDIC SURGICAL SAWS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Aesculap by Aesculap AG — 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
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (1)

  • EUDAMED 758b1d23-2a38-4b72-ade9-069435dcf518 61 fields · synced May 23, 2026