Taiwan FDA registration 03093be52a450a1ac42af44335219f1c

"Hengxin" Schulit blood collection needle (sterilized)

TW: “衡欣”舒利特採血針 (滅菌)

Taiwan·Risk Class 1·TIANJIN HUAHONG TECHNOLOGY CO., LTD.·Registered Feb 14, 2014 – Feb 14, 2024Cancelled

Registration details

Analysis ID: 03093be52a450a1ac42af44335219f1c
Customs Code: DHA09600207007

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: Input;; QMS/QSD

Dates and status

Registration Date: Feb 14, 2014
Expiry Date: Feb 14, 2024
Cancellation Date: Jun 30, 2022

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Hengxin" Schulit 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 03093be52a450a1ac42af44335219f1c and manufactured by TIANJIN HUAHONG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Hengxin Medical Equipment Co., Ltd.

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