Taiwan FDA registration 954787fa82e984034ef3bec6644c7d49
"Schiff" Corrective spectacle lens (Non-Sterile)
TW: "一協紀" 矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·WENZHOU EYEWORKS IMP. & EXP. CO, LTD·Registered Oct 06, 2022 – Oct 06, 2027ActiveRegistration details
- Analysis ID
- 954787fa82e984034ef3bec6644c7d49
- License Form
- Ministry of Health Medical Device Land Transport No. 004679
- Customs Code
- DHA09600467907
Company information
- Manufacturer
- WENZHOU EYEWORKS IMP. & EXP. CO, LTD
- Manufacturer Country
- China
- Authorized Representative
- SCHIFF INTERNATIONAL CO.
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)
- M5844 corrective lenses
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Oct 06, 2022
- Expiry Date
- Oct 06, 2027
About this record
Access comprehensive regulatory information for "Schiff" Corrective spectacle lens (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 954787fa82e984034ef3bec6644c7d49 and manufactured by WENZHOU EYEWORKS IMP. & EXP. CO, LTD. The authorized representative in Taiwan is SCHIFF INTERNATIONAL CO..
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