Taiwan FDA registration aeff320036ac861286c3af0d2aa6b1dc
miacare DELiGHT 1-Day Contact Lens with EautraSil Plus
TW: 美若康沐氧日拋型矽水膠隱形眼鏡
Registration details
- Analysis ID
- aeff320036ac861286c3af0d2aa6b1dc
- License Form
- Ministry of Health Medical Device Manufacturing No. 007471
Company information
- Manufacturer
- BenQ Materials Co., Ltd. Taoyuan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BENQ MATERIALS CORP.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M5925 Flexible Contact Lens
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 19, 2022
- Expiry Date
- May 19, 2027
About this record
Access comprehensive regulatory information for miacare DELiGHT 1-Day Contact Lens with EautraSil Plus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aeff320036ac861286c3af0d2aa6b1dc and manufactured by BenQ Materials Co., Ltd. Taoyuan Factory. The authorized representative in Taiwan is BENQ MATERIALS CORP..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices