"PENTAX" corrective spectacle lens (Non-Sterile)
Taiwan·Risk Class 1·MD·HOYA LENS THAILAND LTD.·Registered Sep 27, 2017 – Sep 27, 2027Active- Analysis ID
- 70998c2c9c75b8232b4a030cad768068
- License Form
- Ministry of Health Medical Device Import No. 018357
- Customs Code
- DHA09401835708
- Manufacturer
- HOYA LENS THAILAND LTD.
- Manufacturer Country
- Thailand
- 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
- Imported from abroad
- Registration Date
- Sep 27, 2017
- Expiry Date
- Sep 27, 2027
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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 70998c2c9c75b8232b4a030cad768068 and manufactured by HOYA LENS THAILAND 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 TAIWAN 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.