Taiwan FDA registration 322acbe72b81f02000470cc3092fda66

Fol sterilized blood lancets

TW: 福爾滅菌採血針

Taiwan·Risk Class 1·TIANJIN HUAHONG TECHNOLOGY CO., LTD.·Registered May 13, 2019 – May 13, 2029Active

Registration details

Analysis ID: 322acbe72b81f02000470cc3092fda66
Customs Code: DHA09600379300

Company information

Manufacturer: TIANJIN HUAHONG TECHNOLOGY CO., LTD.
Manufacturer Country: China
Authorized Representative: TAIDOC TECHNOLOGY 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: QMS/QSD;; Input;; Chinese goods

Dates and status

Registration Date: May 13, 2019
Expiry Date: May 13, 2029

About this record

Access comprehensive regulatory information for Fol sterilized blood lancets in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 322acbe72b81f02000470cc3092fda66 and manufactured by TIANJIN HUAHONG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is TAIDOC TECHNOLOGY 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.