SILOR Corrective Spectacle Lens (Non-sterile)
Taiwan·Risk Class 1·MD·ESSILOR MANUFACTURING (THAILAND) CO., LTD.·Registered Sep 29, 2017 – Sep 29, 2022Expired- Analysis ID
- 5bda46133132b9e620c7a30f33f5b31a
- License Form
- Ministry of Health Medical Device Import No. 018363
- Customs Code
- DHA09401836303
- Manufacturer
- ESSILOR MANUFACTURING (THAILAND) CO., LTD.
- Manufacturer Country
- Thailand
- Authorized Representative
- ESSILOR-POLYLITE TAIWAN CO., LTD.
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5844 corrective lenses
- Import Information
- Imported from abroad
- Registration Date
- Sep 29, 2017
- Expiry Date
- Sep 29, 2022
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Access comprehensive regulatory information for SILOR 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 5bda46133132b9e620c7a30f33f5b31a and manufactured by ESSILOR MANUFACTURING (THAILAND) CO., LTD.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ESSILOR-POLYLITE TAIWAN CO., LTD., and 1 recent registrations in the same category. 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.