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"Taixin" blood collection pen (unsterilized) - Taiwan Registration fe5d0994304ce90912c728a3fe0fca4b

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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fe5d0994304ce90912c728a3fe0fca4b
Registration Details
Taiwan FDA Registration: fe5d0994304ce90912c728a3fe0fca4b
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Device Details

"Taixin" blood collection pen (unsterilized)
TW: "ๅฐๆฌฃ" ๆŽก่ก€็ญ†(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

fe5d0994304ce90912c728a3fe0fca4b

DHA09600255100

Company Information

Product Details

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.

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

Chinese goods;; input

Dates and Status

Nov 13, 2015

Nov 13, 2025

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