AIR OPTIX Night & Day (UDI-DI: 038065GMN000116GX); AQUA (lotrafilcon A) (UDI-DI: 038065GMN000117GZ)

Albania medical device registration · Alcon Laboratories, Inc. 6201 South Freeway, Forth Worth, Texas 76134-2099 USA · IIb · Model AIR OPTIX Night & Day (UDI-DI: 038065GMN000116GX); AQUA (lotrafilcon A) (UDI-DI: 038065GMN000117GZ) · Registered September 22, 2022

Device classification

Risk Class: IIb
Product Model: AIR OPTIX Night & Day (UDI-DI: 038065GMN000116GX); AQUA (lotrafilcon A) (UDI-DI: 038065GMN000117GZ)
Product Name: AIR OPTIX Night & Day (UDI-DI: 038065GMN000116GX); AQUA (lotrafilcon A) (UDI-DI: 038065GMN000117GZ)

Registration information

Registration Date: September 22, 2022
Analysis ID: 12820

Manufacturer

Name: Alcon Laboratories, Inc. 6201 South Freeway, Forth Worth, Texas 76134-2099 USA

Product information

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About this record

Access comprehensive regulatory information for AIR OPTIX Night & Day (UDI-DI: 038065GMN000116GX); AQUA (lotrafilcon A) (UDI-DI: 038065GMN000117GZ) in the Albania medical device market through Pure Global AI's free database. This IIb medical device is manufactured by Alcon Laboratories, Inc. 6201 South Freeway, Forth Worth, Texas 76134-2099 USA. The device was registered on September 22, 2022.

This page provides complete registration details including product model (AIR OPTIX Night & Day (UDI-DI: 038065GMN000116GX); AQUA (lotrafilcon A) (UDI-DI: 038065GMN000117GZ)), manufacturer information, risk classification, and regulatory compliance data from the official Albania medical device database. Pure Global AI offers free access to Albania's medical device registry, helping global MedTech companies navigate Albania regulations efficiently.