Taiwan FDA registration 410540f5893344ca92e8b82a1602ad5a

Execom Tissue Chopper (Sterilization)

TW: 安切康組織切碎機(滅菌)

Taiwan·Risk Class 1·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Apr 09, 2019 – Apr 09, 2029Active

Registration details

Analysis ID: 410540f5893344ca92e8b82a1602ad5a

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: QMS/QSD;; 國產;; 委託製造

Dates and status

Registration Date: Apr 09, 2019
Expiry Date: Apr 09, 2029

About this record

Access comprehensive regulatory information for Execom Tissue Chopper (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 410540f5893344ca92e8b82a1602ad5a and manufactured by YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is BIOGEND THERAPEUTICS CO., LTD..

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