SHINOBI Corrective Spectacle Lens (Non-Sterile)
Taiwan·Risk Class 1·MD·DAE MYUNG OPTICAL CO., LTD·Registered Feb 02, 2021 – Feb 02, 2026Expired- Analysis ID
- f0275e59452b94d5335e39a1b224f46d
- License Form
- Ministry of Health Medical Device Import No. 022288
- Customs Code
- DHA09402228804
- Manufacturer
- DAE MYUNG 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 02, 2021
- Expiry Date
- Feb 02, 2026
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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 f0275e59452b94d5335e39a1b224f46d and manufactured by DAE MYUNG OPTICAL CO., LTD. The authorized representative in Taiwan is Mahkota Eyewear Limited.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including 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.