Taiwan FDA registration b314527bf4d876cb24c85215b62345ff
Fujita Corrective Spectacle Lens (Non-Sterile)
TW: 藤田 矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·FUJITA OPTICAL CO., LTD.·Registered Apr 08, 2016 – Apr 08, 2021CancelledRegistration details
- Analysis ID
- b314527bf4d876cb24c85215b62345ff
- License Form
- Ministry of Health Medical Device Import No. 016368
- Customs Code
- DHA09401636803
Company information
- Manufacturer
- FUJITA OPTICAL CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- EMIN OPTICAL CO., LTD.
Product details
- 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, 2016
- Expiry Date
- Apr 08, 2021
- Cancellation Date
- Aug 31, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Fujita 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 b314527bf4d876cb24c85215b62345ff and manufactured by FUJITA OPTICAL CO., LTD.. The authorized representative in Taiwan is EMIN OPTICAL 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