Taiwan FDA registration d4bb58d027dc76f18d5e71e2a279e691
NGK Corrective Spectacle Lens(Non-Sterile)
TW: 日本眼鏡光學 矯正鏡片(未滅菌)
Registration details
- Analysis ID
- d4bb58d027dc76f18d5e71e2a279e691
- License Form
- Ministry of Health Medical Device Import No. 022454
- Customs Code
- DHA09402245408
Company information
- Manufacturer
- NIPPON OPHTHALMIC CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- HKO OPTICAL LENS (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
- Apr 08, 2021
- Expiry Date
- Apr 08, 2026
About this record
Access comprehensive regulatory information for NGK 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 d4bb58d027dc76f18d5e71e2a279e691 and manufactured by NIPPON OPHTHALMIC CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (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