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Taixin blood collection needle (sterilized) - Taiwan Registration d24c209420100199fa9abf3ba357a308

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.

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d24c209420100199fa9abf3ba357a308
Registration Details
Taiwan FDA Registration: d24c209420100199fa9abf3ba357a308
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Device Details

Taixin blood collection needle (sterilized)
TW: ๅฐๆฌฃๆŽก่ก€้‡(ๆป…่Œ)
Risk Class 1

Registration Details

d24c209420100199fa9abf3ba357a308

DHA09600200101

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

Input;; QMS/QSD;; Chinese goods

Dates and Status

Oct 14, 2013

Oct 14, 2028

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