Taiwan FDA registration fe5d0994304ce90912c728a3fe0fca4b

"Taixin" blood collection pen (unsterilized)

TW: "台欣" 採血筆(未滅菌)
Taiwan flagTaiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Nov 13, 2015 – Nov 13, 2025Expired
Registration details
Analysis ID
fe5d0994304ce90912c728a3fe0fca4b
Customs Code
DHA09600255100
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
Chinese goods;; input
Dates and status
Registration Date
Nov 13, 2015
Expiry Date
Nov 13, 2025
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About this record

Access comprehensive regulatory information for "Taixin" blood collection pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe5d0994304ce90912c728a3fe0fca4b 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 BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD., and 2 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.

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