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Snapshot 2026-10-11 · Link to EUDAMED

Neoss® Guide Kit System Box

UDI-DI 05060440337505Basic UDI-DI 506044033N0028N7

Class I · MDR · Neoss AB

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

No certificate found.

Snapshot 2026-10-11 · Link to EUDAMED

Manufacturer

Neoss AB

SRN SE-MF-000022321

SE · Göteborg

manufacturer

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Canonical device page: /device/neoss-guide-kit-system-box-7505 · UDI page: /udi/05060440337505

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