Taiwan FDA registration 27f8666b3f9aa06ee73447fdbb8e4a34

Jinhong blood collection needle (sterilized)

TW: 金鴻採血針(滅菌)

Taiwan·Risk Class 1·TIANJIN HUAHONG TECHNOLOGY CO., LTD.·Registered Nov 29, 2021 – Nov 29, 2026Active

Registration details

Analysis ID: 27f8666b3f9aa06ee73447fdbb8e4a34
Customs Code: DHA09600458804

Company information

Manufacturer: TIANJIN HUAHONG TECHNOLOGY CO., LTD.
Manufacturer Country: China
Authorized Representative: Ace Medical Technology 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;; Input;; Chinese goods

Dates and status

Registration Date: Nov 29, 2021
Expiry Date: Nov 29, 2026

About this record

Access comprehensive regulatory information for Jinhong blood collection needle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 27f8666b3f9aa06ee73447fdbb8e4a34 and manufactured by TIANJIN HUAHONG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Ace Medical Technology Co., Ltd..

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