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“Terumo” MEDISAFE FINETOUCH II Lancing Device With Set Lever (Non-Sterile) - Taiwan Registration 315950bd03e7d10e8d7987640468b913

Access comprehensive regulatory information for “Terumo” MEDISAFE FINETOUCH II Lancing Device With Set Lever (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 315950bd03e7d10e8d7987640468b913 and manufactured by KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

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315950bd03e7d10e8d7987640468b913
Registration Details
Taiwan FDA Registration: 315950bd03e7d10e8d7987640468b913
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Device Details

“Terumo” MEDISAFE FINETOUCH II Lancing Device With Set Lever (Non-Sterile)
TW: “泰爾茂”採血筆 (未滅菌)
Risk Class 1
MD

Registration Details

315950bd03e7d10e8d7987640468b913

Ministry of Health Medical Device Import No. 020300

DHA09402030000

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Apr 11, 2019

Apr 11, 2024