Taiwan FDA registration 13e50ac8bec203ac7e49629dcb095b5d

"Huahong" blood collection needle (sterilized)

TW: "樺宏" 採血針(滅菌)

Taiwan·Risk Class 1·TIANJIN HUAHONG TECHNOLOGY CO., LTD.·Registered Apr 14, 2014 – Apr 14, 2029Active

Registration details

Analysis ID: 13e50ac8bec203ac7e49629dcb095b5d
Customs Code: DHA09600211006

Company information

Manufacturer: TIANJIN HUAHONG TECHNOLOGY CO., LTD.
Manufacturer Country: China
Authorized Representative: LIKWANG INSTRUMENTS 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: Chinese goods;; input

Dates and status

Registration Date: Apr 14, 2014
Expiry Date: Apr 14, 2029

About this record

Access comprehensive regulatory information for "Huahong" 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 13e50ac8bec203ac7e49629dcb095b5d and manufactured by TIANJIN HUAHONG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LIKWANG INSTRUMENTS 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.