Taiwan FDA registration ab8fa13e1ea676a507f3512dba30ca70

AURORA Monthly disposable silicone hydrogel contact lens

TW: 歐若拉月拋矽水膠隱形眼鏡

Taiwan·Risk Class 2·MD·HOPE VISION CO., LTD.·Registered Jun 24, 2021 – Jul 03, 2025Expired

Registration details

Analysis ID: ab8fa13e1ea676a507f3512dba30ca70
License Form: Ministry of Health Medical Device Manufacturing No. 007204

Company information

Manufacturer: HOPE VISION CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HOPE VISION CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M5925 Flexible Contact Lens
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Jun 24, 2021
Expiry Date: Jul 03, 2025

About this record

Access comprehensive regulatory information for AURORA Monthly disposable silicone hydrogel contact lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab8fa13e1ea676a507f3512dba30ca70 and manufactured by HOPE VISION CO., LTD.. The authorized representative in Taiwan is HOPE VISION CO., LTD..

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