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UDI Compass
Unknown / Not in EUDAMED

Snapshot 2026-10-13 · Link to EUDAMED

AcrySof IQ Vivity

UDI-DI 00380652426114Basic UDI-DI 038065GMN000132GV

Class IIb · MDR · Alcon Laboratories, Inc.

Identification
Model
—
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 204 other UDI-DIs.

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Canonical device page: /device/acrysof-iq-vivity-6114 · UDI page: /udi/00380652426114

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