Taiwan FDA registration d7f30fae176748eec0ae898c71106c37

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

TW: “優視” 手動式眼科手術器械 (未滅菌)

Taiwan·Risk Class 1·MD·Fine Hub Ophthalmic·Registered May 19, 2020 – May 19, 2025Expired

Registration details

Analysis ID: d7f30fae176748eec0ae898c71106c37
License Form: Ministry of Health Medical Device Import No. 021548
Customs Code: DHA09402154802

Company information

Manufacturer: Fine Hub Ophthalmic
Manufacturer Country: Pakistan
Authorized Representative: AMAZMED CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M4350 Manual Ophthalmic Surgery Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: May 19, 2020
Expiry Date: May 19, 2025

About this record

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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