Taiwan FDA registration 894a84d8480758ec28d5157bf998c888

"Renfei" suture knotting instrument (unsterilized)

TW: “仁斐”縫線打結器械 (未滅菌)

Taiwan·Risk Class 1·RANFAC CORP.·Registered Nov 05, 2009 – Nov 05, 2014Cancelled

Registration details

Analysis ID: 894a84d8480758ec28d5157bf998c888
Customs Code: DHA04400827102

Company information

Manufacturer: RANFAC CORP.
Manufacturer Country: United States
Authorized Representative: MEDLIANCE 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, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Nov 05, 2009
Expiry Date: Nov 05, 2014
Cancellation Date: Apr 25, 2018

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Renfei" suture knotting instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 894a84d8480758ec28d5157bf998c888 and manufactured by RANFAC CORP.. The authorized representative in Taiwan is MEDLIANCE LTD..

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