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Elan 4

EUDAMED

Class IIa (EU MDR)

Ref GP493R

by Aesculap AG

Identity

Trade Name
ELAN 4 EUDAMED
Device Name
ELAN 4 saw blade (RU) EUDAMED
Model / Reference
GP493R EUDAMED

Identifiers

Primary DI / UDI-DI
04046964526978 EUDAMED
Basic UDI-DI
40392390000014592T EUDAMED
EMDN Code
Z12100980 INSTRUMENTS FOR MOTORISED NEUROSURGERY SYSTEMS - HARDWARE ACCESSORIES 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

Elan 4 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 83c17a3a-799b-463f-8804-f4786fec430f 61 fields · synced May 23, 2026