Taiwan FDA registration b4d83a25e5c791f7d07a4d4f6c1237fd
Lifu corrective lenses (unsterilized)
TW: 麗富矯正鏡片(未滅菌)
Registration details
- Analysis ID
- b4d83a25e5c791f7d07a4d4f6c1237fd
- Customs Code
- DHA09600458307
Company information
- Manufacturer
- JIANGSU SIGO OPTICAL CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- EYEJING EYEWEAR INC.
Product details
- Intended Use
- Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.5844 corrective lenses
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Nov 12, 2021
- Expiry Date
- Nov 12, 2026
About this record
Access comprehensive regulatory information for Lifu corrective lenses (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b4d83a25e5c791f7d07a4d4f6c1237fd and manufactured by JIANGSU SIGO OPTICAL CO., LTD.. The authorized representative in Taiwan is EYEJING EYEWEAR INC..
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