Unknown / Not in EUDAMED

Snapshot 2026-10-09 · Link to EUDAMED

AcrySof IQ Vivity

UDI-DI 00380652422543Basic UDI-DI 038065GMN000134GZ

Class IIb · MDR · Alcon Laboratories, Inc.

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Identification

Model: —
EMDN: P030102100301
Issuing agency: GS1
Device status: active
Sterile: Yes
Implantable: Yes
Measuring function: No
Reusable surgical: No

Certificates

G70 020895 0397

EU technical documentation assessment · unknown

Notified body: TÜV SÜD Product Service GmbH (0123)

Valid from 2026-06-11 · Expiry 2028-08-29

Scope not stated in certificate data.

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

Manufacturer

Alcon Laboratories, Inc.

SRN US-MF-000016248

US · Fort Worth

manufacturer

Authorised representative: Alcon Laboratories Belgium (BE-AR-000014721)

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Showing 12 of 301 other UDI-DIs.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/acrysof-iq-vivity-2543 · UDI page: /udi/00380652422543

All devices from Alcon Laboratories, Inc.

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