Taiwan FDA registration 896ba0594d8811220852683054390eeb

"Renzi" manual instruments for general surgery (unsterilized)

TW: “仁齊”一般手術用手動式器械(未滅菌)

Taiwan·Risk Class 1·YIDA INSTRUMENT AND EQUIPMENT FACTORY, TONGLU, HANGZHOU·Registered Jan 13, 2012 – Jan 13, 2017Cancelled

Registration details

Analysis ID: 896ba0594d8811220852683054390eeb
Customs Code: DHA04600156408

Company information

Manufacturer: YIDA INSTRUMENT AND EQUIPMENT FACTORY, TONGLU, HANGZHOU
Manufacturer Country: China
Authorized Representative: TOP-BOUND ENTERPRISE 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, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Jan 13, 2012
Expiry Date: Jan 13, 2017
Cancellation Date: Dec 20, 2019

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Renzi" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 896ba0594d8811220852683054390eeb and manufactured by YIDA INSTRUMENT AND EQUIPMENT FACTORY, TONGLU, HANGZHOU. The authorized representative in Taiwan is TOP-BOUND ENTERPRISE CO., LTD..

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