Taiwan FDA registration 6d8c690107b89a79cffd9498a6aa6a88

"Bosheng" manual instrument for general surgery (not sterilized)

TW: "博晟"一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·Yinghong Bucheng Steel Appliance Co., Ltd·Registered Oct 25, 2018 – Oct 25, 2023Expired

Registration details

Analysis ID: 6d8c690107b89a79cffd9498a6aa6a88

Company information

Manufacturer: Yinghong Bucheng Steel Appliance Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BIOGEND THERAPEUTICS CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Oct 25, 2018
Expiry Date: Oct 25, 2023

About this record

Access comprehensive regulatory information for "Bosheng" manual instrument for general surgery (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6d8c690107b89a79cffd9498a6aa6a88 and manufactured by Yinghong Bucheng Steel Appliance Co., Ltd. The authorized representative in Taiwan is BIOGEND THERAPEUTICS CO., LTD..

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