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"SEIKO" corrective spectacle lens (Non-sterile) - Taiwan Registration 2a610a06512a9e202d5d8d709cb3859a

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 2a610a06512a9e202d5d8d709cb3859a and manufactured by SEIKO HOLDINGS CORPORATION. The authorized representative in Taiwan is Tokyo Optical Co., Ltd. Taipei store.

This page provides complete technical specifications, regulatory compliance details. 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.

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2a610a06512a9e202d5d8d709cb3859a
Registration Details
Taiwan FDA Registration: 2a610a06512a9e202d5d8d709cb3859a
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Device Details

"SEIKO" corrective spectacle lens (Non-sterile)
TW: "็ฒพๅŠŸ" ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2a610a06512a9e202d5d8d709cb3859a

Ministry of Health Medical Device Import No. 017175

DHA09401717500

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

Nov 15, 2016

Nov 15, 2021