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"Snowden Pencer" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration f44bdab81fd903b3c44ab8ee45333863

Access comprehensive regulatory information for "Snowden Pencer" Manual surgical instrument for general use (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 f44bdab81fd903b3c44ab8ee45333863 and manufactured by CAREFUSION. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..

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f44bdab81fd903b3c44ab8ee45333863
Registration Details
Taiwan FDA Registration: f44bdab81fd903b3c44ab8ee45333863
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Device Details

"Snowden Pencer" Manual surgical instrument for general use (Non-Sterile)
TW: "ๅฒ่ซพ้ “่ณ“ๅฃซ" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f44bdab81fd903b3c44ab8ee45333863

Ministry of Health Medical Device Import No. 016951

DHA09401695100

Company Information

United States

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

Sep 02, 2016

Sep 02, 2021