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UDI Compass

Spex

No Certificate Found

Snapshot 2026-10-31 · Link to EUDAMED

UDI-DI 09420082637436Basic UDI-DI 94200517CUSHIONPP

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Class I · MDR · Spex Ltd

Identification

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

Certificates

No certificate found.

Snapshot 2026-10-31 · Link to EUDAMED

Manufacturer

Spex Ltd

SRN NZ-MF-000009327

NZ · Rolleston

manufacturer

Authorised representative: BEO MedConsulting Berlin GmbH (DE-AR-000006764)

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Showing 12 of 4884 other UDI-DIs.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/spex-7436 · UDI page: /udi/09420082637436

All devices from Spex Ltd