Taiwan FDA registration 5e5a04a9f26101b70bd245affc8dd8ee

"Ichikyoki" blood collection needle (sterile)

TW: “一協紀” 採血針 (滅菌)

Taiwan·Risk Class 1·HTL-STREFA S.A.·Registered Apr 15, 2021 – Apr 15, 2026Expired

Registration details

Analysis ID: 5e5a04a9f26101b70bd245affc8dd8ee
Customs Code: DHA09402248608

Company information

Manufacturer: HTL-STREFA S.A.
Manufacturer Country: Poland
Authorized Representative: SCHIFF INTERNATIONAL CO.

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

Dates and status

Registration Date: Apr 15, 2021
Expiry Date: Apr 15, 2026

About this record

Access comprehensive regulatory information for "Ichikyoki" blood collection needle (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5e5a04a9f26101b70bd245affc8dd8ee and manufactured by HTL-STREFA S.A.. The authorized representative in Taiwan is SCHIFF INTERNATIONAL CO..

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.