Taiwan FDA registration e3b2b0d3c0b8f35922b22153c4e4674f

Didas Vacuum Blood Collection System (Sterilization)

TW: "諦達思" 真空血液收集系統 (滅菌)

Taiwan·Risk Class 1·ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD.·Registered Jul 24, 2017 – Jul 24, 2027Active

Registration details

Analysis ID: e3b2b0d3c0b8f35922b22153c4e4674f
Customs Code: DHA09600315701

Company information

Manufacturer: ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD.
Manufacturer Country: China
Authorized Representative: AGREE HEALTH CARE TECHNOLOGY, LTD.

Product details

Intended Use: Limited to the first level identification range of the "Vacuum Blood Collection System (B.9125)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.9125 Vacuum blood collection system
Import Information: Input;; QMS/QSD;; Chinese goods

Dates and status

Registration Date: Jul 24, 2017
Expiry Date: Jul 24, 2027

About this record

Access comprehensive regulatory information for Didas Vacuum Blood Collection System (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e3b2b0d3c0b8f35922b22153c4e4674f and manufactured by ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, LTD..

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