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“Fine Hub Ophthalmic” Manual ophthalmic surgical instrument (Non-Sterile) - Taiwan Registration d7f30fae176748eec0ae898c71106c37

Access comprehensive regulatory information for “Fine Hub Ophthalmic” Manual ophthalmic surgical instrument (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 d7f30fae176748eec0ae898c71106c37 and manufactured by Fine Hub Ophthalmic. The authorized representative in Taiwan is AMAZMED CO., LTD..

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d7f30fae176748eec0ae898c71106c37
Registration Details
Taiwan FDA Registration: d7f30fae176748eec0ae898c71106c37
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Device Details

“Fine Hub Ophthalmic” Manual ophthalmic surgical instrument (Non-Sterile)
TW: “優視” 手動式眼科手術器械 (未滅菌)
Risk Class 1
MD

Registration Details

d7f30fae176748eec0ae898c71106c37

Ministry of Health Medical Device Import No. 021548

DHA09402154802

Company Information

Pakistan

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".

M Ophthalmic devices

M4350 Manual Ophthalmic Surgery Instrument

Imported from abroad

Dates and Status

May 19, 2020

May 19, 2025