Taiwan FDA registration d24c209420100199fa9abf3ba357a308

Taixin blood collection needle (sterilized)

TW: 台欣採血針(滅菌)
Taiwan flagTaiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Oct 14, 2013 – Oct 14, 2028Active
Registration details
Analysis ID
d24c209420100199fa9abf3ba357a308
Customs Code
DHA09600200101
Company information
Manufacturer Country
China
Authorized Representative
TYSON BIORESEARCH INC.
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
Oct 14, 2013
Expiry Date
Oct 14, 2028
Companies making similar products

Top companies providing products similar to "Taixin blood collection needle (sterilized)"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for Taixin 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 d24c209420100199fa9abf3ba357a308 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is TYSON BIORESEARCH INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STERILANCE MEDICAL (SUZHOU) INC., and 1 recent registrations in the same category. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations