"PENTAX" corrective spectacle lens (Non-Sterile)
Taiwan·Risk Class 1·MD·HOYA LENS TAIWAN LTD.·Registered Dec 07, 2018 – Dec 07, 2028Active- Analysis ID
- 282d63f6d9174f03f2372c6125a4f5b6
- License Form
- Ministry of Health Medical Device Manufacturing No. 007560
- Manufacturer
- HOYA LENS TAIWAN LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HOYA LENS TAIWAN 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
- Produced in Taiwan, China
- Registration Date
- Dec 07, 2018
- Expiry Date
- Dec 07, 2028
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Access comprehensive regulatory information for "PENTAX" 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 282d63f6d9174f03f2372c6125a4f5b6 and manufactured by HOYA LENS TAIWAN LTD.. The authorized representative in Taiwan is HOYA LENS TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including HOYA LENS MANUFACTURING MALAYSIA SDN.BHD., HOYA LENS THAILAND LTD., and 2 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.