"PENTAX" corrective spectacle lens (Non-Sterile)
Taiwan·Risk Class 1·MD·HOYA LENS MANUFACTURING MALAYSIA SDN.BHD.·Registered Oct 06, 2017 – Oct 06, 2022Expired- Analysis ID
- eda12e5fce1cd778921844e4f78f3198
- License Form
- Ministry of Health Medical Device Import No. 018385
- Customs Code
- DHA09401838500
- Manufacturer
- HOYA LENS MANUFACTURING MALAYSIA SDN.BHD.
- Manufacturer Country
- Malaysia
- 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
- Oct 06, 2017
- Expiry Date
- Oct 06, 2022
Top companies providing products similar to ""PENTAX" corrective spectacle lens (Non-Sterile)"
Recently registered similar products
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 eda12e5fce1cd778921844e4f78f3198 and manufactured by HOYA LENS MANUFACTURING MALAYSIA SDN.BHD.. 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 TAIWAN LTD., 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.