Taiwan FDA registration bf33d8694e231d91663c806303028689

"Hengxin" Quick Test Blood Collection Pen (Unsterilized)

TW: "衡欣" 快測採血筆 (未滅菌)

Taiwan·Risk Class 1·TIANJIN HUAHONG TECHNOLOGY CO., LTD.·Registered Apr 20, 2017 – Apr 20, 2022Cancelled

Registration details

Analysis ID: bf33d8694e231d91663c806303028689
Customs Code: DHA09600306802

Company information

Manufacturer: TIANJIN HUAHONG TECHNOLOGY CO., LTD.
Manufacturer Country: China
Authorized Representative: Hengxin Medical Equipment Co., Ltd

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Chinese goods;; input

Dates and status

Registration Date: Apr 20, 2017
Expiry Date: Apr 20, 2022
Cancellation Date: Jun 15, 2022

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Hengxin" Quick Test Blood Collection Pen (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bf33d8694e231d91663c806303028689 and manufactured by TIANJIN HUAHONG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Hengxin Medical Equipment Co., Ltd.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.