Taiwan FDA registration efb46451f63bc6b8d347e3b58c02d48b
“Nikon” Corrective Spectacle Lens (Non-sterile)
TW: “尼康” 矯正鏡片(未滅菌)
Taiwan·Risk Class 1·MD·Essilor Hong Kong Ltd.·Registered Sep 04, 2018 – Sep 04, 2028ActiveRegistration details
- Analysis ID
- efb46451f63bc6b8d347e3b58c02d48b
- License Form
- Ministry of Health Medical Device Import No. 019568
- Customs Code
- DHA09401956800
Company information
- Manufacturer
- Essilor Hong Kong Ltd.
- Manufacturer Country
- Hong Kong
- Authorized Representative
- ESSILOR-POLYLITE TAIWAN CO., LTD.
Product details
- 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
Dates and status
- Registration Date
- Sep 04, 2018
- Expiry Date
- Sep 04, 2028
About this record
Access comprehensive regulatory information for “Nikon” 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 efb46451f63bc6b8d347e3b58c02d48b and manufactured by Essilor Hong Kong Ltd.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN 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.
Free DatabasePowered by Pure Global AI89,000+ Devices