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Snapshot 2026-10-09 · Link to EUDAMED

IQ E.MOTION PRO

UDI-DI 04046964121708Basic UDI-DI 40392390000020872K

Class IIa · MDR · Aesculap AG

Identification
Model
—
Issuing agency
GS1
Device status
active
Sterile
No
Implantable
No
Measuring function
No
Reusable surgical
No
Certificates

No certificate found.

Snapshot 2026-10-09 · Link to EUDAMED

Manufacturer

Aesculap AG

SRN DE-MF-000005504

DE · Tuttlingen

manufacturer

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Canonical device page: /device/iq-e-motion-pro-1708 · UDI page: /udi/04046964121708

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