Taiwan FDA registration e497084410c7f36af6891b3c8c6903ee
Pure Plus Silicone Hydrogel Daily Contact Lens
TW: 純粹氧水潤高透氧矽水膠日拋隱形眼鏡
Taiwan·Risk Class 2·MD·YUNG SHENG OPTICAL CO., LTD.·Registered Jul 14, 2023 – Jul 14, 2028ActiveRegistration details
- Analysis ID
- e497084410c7f36af6891b3c8c6903ee
- License Form
- Ministry of Health Medical Device Manufacturing No. 007905
Company information
- Manufacturer
- YUNG SHENG OPTICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Yung Sheng Optical Co., Ltd. Xindian Branch
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
- Jul 14, 2023
- Expiry Date
- Jul 14, 2028
About this record
Access comprehensive regulatory information for Pure Plus Silicone Hydrogel Daily 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 e497084410c7f36af6891b3c8c6903ee and manufactured by YUNG SHENG OPTICAL CO., LTD.. The authorized representative in Taiwan is Yung Sheng Optical Co., Ltd. Xindian Branch.
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