Taiwan FDA registration 76aebcea8c63464ee7cfd1ca564a505f

"Bo Sheng" tissue chopper (unsterilized)

TW: “博晟”組織切碎機(未滅菌)

Taiwan·Risk Class 1·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Nov 21, 2018 – Nov 21, 2023Expired

Registration details

Analysis ID: 76aebcea8c63464ee7cfd1ca564a505f

Company information

Manufacturer: YUNG KANG MEDICAL DEVICE TECHNOLOGY 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: Nov 21, 2018
Expiry Date: Nov 21, 2023

About this record

Access comprehensive regulatory information for "Bo Sheng" tissue chopper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 76aebcea8c63464ee7cfd1ca564a505f and manufactured by YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is BIOGEND THERAPEUTICS CO., LTD..

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