SHINOBI Corrective Spectacle Lens (Non-Sterile)
Taiwan·Risk Class 1·MD·DAEMYUNG OPTICAL CO., LTD·Registered Feb 23, 2016 – Feb 23, 2021Expired- Analysis ID
- 8068a436d8b4aad57980acbcd71a4f10
- License Form
- Ministry of Health Medical Device Import No. 016182
- Customs Code
- DHA09401618202
- Manufacturer
- DAEMYUNG OPTICAL CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Mahkota Eyewear Limited
- 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
- Feb 23, 2016
- Expiry Date
- Feb 23, 2021
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Access comprehensive regulatory information for SHINOBI 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 8068a436d8b4aad57980acbcd71a4f10 and manufactured by DAEMYUNG OPTICAL CO., LTD. The authorized representative in Taiwan is Mahkota Eyewear Limited.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including DAE MYUNG OPTICAL CO., LTD, DAEMYUNG OPTICAL CO., 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.