No Certificate Found

Snapshot 2026-10-17 · Link to EUDAMED

Compresse lin universelle kinedolin

UDI-DI 06192313400012Basic UDI-DI 6192313400018T

Class I · MDR · KINE L'AYPTIS LABO

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Identification

Model: kinedolin
EMDN: M9001
Issuing agency: GS1
Device status: active
Sterile: No
Implantable: No
Measuring function: No
Reusable surgical: No

Certificates

No certificate found.

Snapshot 2026-10-17 · Link to EUDAMED

Manufacturer

KINE L'AYPTIS LABO

SRN TN-MF-000020714

TN · Lamta

manufacturer

Authorised representative: kipocora (FR-AR-000017148)

Related UDI-DIs

No other UDI-DIs share this Basic UDI-DI in this snapshot.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/compresse-lin-universelle-kinedolin-0012 · UDI page: /udi/06192313400012

All devices from KINE L'AYPTIS LABO

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