Taiwan FDA registration fe8ef7da165736f2dd8c3b886e344023

"Ruikang" blood collection needle (sterilization)

TW: "睿康"採血針(滅菌)

Taiwan·Risk Class 1·TIANJIN HUAHONG TECHNOLOGY CO.,LTD·Registered Apr 13, 2015 – Apr 13, 2025Expired

Registration details

Analysis ID: fe8ef7da165736f2dd8c3b886e344023
Customs Code: DHA09600236401

Company information

Manufacturer: TIANJIN HUAHONG TECHNOLOGY CO.,LTD
Manufacturer Country: China
Authorized Representative: MEDIFUN CORPORATION

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: Input;; QMS/QSD;; Chinese goods

Dates and status

Registration Date: Apr 13, 2015
Expiry Date: Apr 13, 2025

About this record

Access comprehensive regulatory information for "Ruikang" blood collection needle (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe8ef7da165736f2dd8c3b886e344023 and manufactured by TIANJIN HUAHONG TECHNOLOGY CO.,LTD. The authorized representative in Taiwan is MEDIFUN CORPORATION.

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.