Taiwan FDA registration e488c7dc34d41ee7519b046f33904a43
SEESCAN Daily Disposable Silicone Hydrogel Contact Lens
TW: 矽視康日拋矽水膠隱形眼鏡
Registration details
- Analysis ID
- e488c7dc34d41ee7519b046f33904a43
- License Form
- Ministry of Health Medical Device Manufacturing No. 007318
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
- Oct 25, 2021
- Expiry Date
- Mar 12, 2024
About this record
Access comprehensive regulatory information for SEESCAN Daily 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 e488c7dc34d41ee7519b046f33904a43 and manufactured by HOPE VISION CO., LTD.. The authorized representative in Taiwan is HOPE VISION CO., LTD..
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.
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