“SEIKO” Corrective spectacle lens (Non-Sterile)
Taiwan·Risk Class 1·MD·EHS LENS PHILIPPINES, INC.·Registered Oct 16, 2019 – Oct 16, 2024Expired- Analysis ID
- f246ec08c20f11a04f00cf9b627cff33
- License Form
- Ministry of Health Medical Device Import No. 020952
- Customs Code
- DHA09402095201
- Manufacturer
- EHS LENS PHILIPPINES, INC.
- Manufacturer Country
- Philippines
- Authorized Representative
- MEGANEICHIBA TAIWAN CO., LTD.
- 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
- Registration Date
- Oct 16, 2019
- Expiry Date
- Oct 16, 2024
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Access comprehensive regulatory information for “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 f246ec08c20f11a04f00cf9b627cff33 and manufactured by EHS LENS PHILIPPINES, INC.. The authorized representative in Taiwan is MEGANEICHIBA TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOYA VISION CARE COMPANY, and 1 recent registrations in the same category. 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.