Taiwan FDA registration 3835a7ca8f1cd0f3d9e4c7eca1c9a329
L'elan Corrective Spectacle Lens (Non-Sterile)
TW: "樂齡" 矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·IKEDA LENS INDUSTRY CO., LTD·Registered Jan 28, 2014 – Jan 28, 2019CancelledRegistration details
- Analysis ID
- 3835a7ca8f1cd0f3d9e4c7eca1c9a329
- License Form
- Ministry of Health Medical Device Import No. 013818
- Customs Code
- DHA09401381806
Company information
- Manufacturer
- IKEDA LENS INDUSTRY CO., LTD
- Manufacturer Country
- Japan
- Authorized Representative
- L'ELAN ENTERPRISE 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
- Jan 28, 2014
- Expiry Date
- Jan 28, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for L'elan 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 3835a7ca8f1cd0f3d9e4c7eca1c9a329 and manufactured by IKEDA LENS INDUSTRY CO., LTD. The authorized representative in Taiwan is L'ELAN ENTERPRISE CO., LTD..
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