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

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.

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Albania Official Data
IIb
AIR OPTIX Night & Day (UDI-DI: 038065GMN000116GX); AQUA (lotrafilcon A) (UDI-DI: 038065GMN000117GZ)
Albania Medical Device Registration
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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