Taiwan FDA registration b45cc3adbbe350f230c27460901452af
HOYA SEIKO Corrective Spectacle Lens (Non-Sterile)
TW: 豪雅精工 矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·EHS LENS PHILIPPINES, INC.·Registered Jan 13, 2021 – Jan 13, 2026ExpiredRegistration details
- Analysis ID
- b45cc3adbbe350f230c27460901452af
- License Form
- Ministry of Health Medical Device Import No. 022244
- Customs Code
- DHA09402224400
Company information
- Manufacturer
- EHS LENS PHILIPPINES, INC.
- Manufacturer Country
- Philippines
- Authorized Representative
- HOYA LENS TAIWAN 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
- Jan 13, 2021
- Expiry Date
- Jan 13, 2026
About this record
Access comprehensive regulatory information for HOYA SEIKO 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 b45cc3adbbe350f230c27460901452af and manufactured by EHS LENS PHILIPPINES, INC.. The authorized representative in Taiwan is HOYA LENS TAIWAN LTD..
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