Taiwan FDA registration 9d27f2706cb4e34e1a9c65cccfe6b0a6
"ZEITO" CORRECTIVE SPECTACLE LENS (Non-Sterile)
TW: "洅鈄" 矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·ZEITO PLASTIC COMPONENTS SDN BHD·Registered Aug 31, 2016 – Aug 31, 2021ExpiredRegistration details
- Analysis ID
- 9d27f2706cb4e34e1a9c65cccfe6b0a6
- License Form
- Ministry of Health Medical Device Import No. 016942
- Customs Code
- DHA09401694209
Company information
- Manufacturer
- ZEITO PLASTIC COMPONENTS SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- ARGUS VISION INTERNATIONAL LIMITED
Product details
- 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
Dates and status
- Registration Date
- Aug 31, 2016
- Expiry Date
- Aug 31, 2021
About this record
Access comprehensive regulatory information for "ZEITO" 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 9d27f2706cb4e34e1a9c65cccfe6b0a6 and manufactured by ZEITO PLASTIC COMPONENTS SDN BHD. The authorized representative in Taiwan is ARGUS VISION INTERNATIONAL LIMITED.
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