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"ZEITO" CORRECTIVE SPECTACLE LENS (Non-Sterile) - Taiwan Registration 9d27f2706cb4e34e1a9c65cccfe6b0a6

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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9d27f2706cb4e34e1a9c65cccfe6b0a6
Registration Details
Taiwan FDA Registration: 9d27f2706cb4e34e1a9c65cccfe6b0a6
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Device Details

"ZEITO" CORRECTIVE SPECTACLE LENS (Non-Sterile)
TW: "ๆด…้ˆ„" ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9d27f2706cb4e34e1a9c65cccfe6b0a6

Ministry of Health Medical Device Import No. 016942

DHA09401694209

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Aug 31, 2016

Aug 31, 2021