Certificate valid

Snapshot 2026-10-09 · Link to EUDAMED

ASPIFLEX

UDI-DI 08055348434972Basic UDI-DI 805534843FT04ASPCY

Class IIa · MDR · Meika Group S.r.l.

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Identification

Model: ASPIFLEX
EMDN: K01020110
Issuing agency: GS1
Device status: active
Sterile: Yes
Implantable: No
Measuring function: No
Reusable surgical: No

Certificates

0425-MDR-030144-00

EU quality management system · valid

Notified body: ICIM S.P.A. (0425)

Valid from 2025-09-10 · Expiry 2030-09-09

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

Meika Group S.r.l.

SRN IT-MF-000029106

IT · Mirandola

manufacturer

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Showing 12 of 77 other UDI-DIs.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/aspiflex-4972 · UDI page: /udi/08055348434972

All devices from Meika Group S.r.l.

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