Taiwan FDA registration f44bdab81fd903b3c44ab8ee45333863

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

TW: "史諾頓賓士" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·CAREFUSION·Registered Sep 02, 2016 – Sep 02, 2021Expired

Registration details

Analysis ID: f44bdab81fd903b3c44ab8ee45333863
License Form: Ministry of Health Medical Device Import No. 016951
Customs Code: DHA09401695100

Company information

Manufacturer: CAREFUSION
Manufacturer Country: United States
Authorized Representative: DOUBLE-SUCCESS CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4800 General Surgery Manual Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Sep 02, 2016
Expiry Date: Sep 02, 2021

About this record

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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