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“OSA” corrective spectacle lens (Non-Sterile) - Taiwan Registration 5683e2c725cdfd049da57ac73a9a17c5

Access comprehensive regulatory information for “OSA” 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 5683e2c725cdfd049da57ac73a9a17c5 and manufactured by Tainan Factory of Taiwan Branch of Singapore Shangtiange Technology Co., Ltd. The authorized representative in Taiwan is TGT HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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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5683e2c725cdfd049da57ac73a9a17c5
Registration Details
Taiwan FDA Registration: 5683e2c725cdfd049da57ac73a9a17c5
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Device Details

“OSA” corrective spectacle lens (Non-Sterile)
TW: “歐薩”矯正鏡片(未滅菌)
Risk Class 1
MD

Registration Details

5683e2c725cdfd049da57ac73a9a17c5

Ministry of Health Medical Device Manufacturing No. 007674

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

Produced in Taiwan, China

Dates and Status

Mar 12, 2019

Mar 12, 2024