“SEIKO” Corrective spectacle lens (Non-Sterile)
Taiwan·Risk Class 1·MD·HOYA VISION CARE COMPANY·Registered Oct 16, 2019 – Oct 16, 2024Expired- Analysis ID
- 9f58a17cb47c818ecf4b0589936c05ea
- License Form
- Ministry of Health Medical Device Import No. 020951
- Customs Code
- DHA09402095102
- Manufacturer
- HOYA VISION CARE COMPANY
- Manufacturer Country
- Japan
- Authorized Representative
- MEGANEICHIBA TAIWAN CO., 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 16, 2019
- Expiry Date
- Oct 16, 2024
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Access comprehensive regulatory information for “SEIKO” 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 9f58a17cb47c818ecf4b0589936c05ea and manufactured by HOYA VISION CARE COMPANY. The authorized representative in Taiwan is MEGANEICHIBA TAIWAN CO., LTD..
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