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Snapshot 2026-10-09 · Link to EUDAMED

II.,PROMAX,AG,4N protiskluz.lem,tělová

UDI-DI 08591285281908Basic UDI-DI 8591285AGLP22F

Class I · MDR · MAXIS a.s.

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

MAXIS a.s.

SRN CZ-MF-000000989

CZ · Praha 2

manufacturer

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Canonical device page: /device/ii-promax-ag-4n-protiskluz-lem-telova-1908 · UDI page: /udi/08591285281908

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