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"Lexia" blood collection needle (sterilization) - Taiwan Registration 9f011a9a08e2bf446b4483ddcb28cbf4

Access comprehensive regulatory information for "Lexia" blood collection needle (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f011a9a08e2bf446b4483ddcb28cbf4 and manufactured by Shandong Lianfa Medical Plastic Products Co., Ltd.. The authorized representative in Taiwan is LUVNSHARE BIOMEDICAL, INC..

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.

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9f011a9a08e2bf446b4483ddcb28cbf4
Registration Details
Taiwan FDA Registration: 9f011a9a08e2bf446b4483ddcb28cbf4
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Device Details

"Lexia" blood collection needle (sterilization)
TW: โ€œๆจ‚ๅ”โ€ๆŽก่ก€้‡(ๆป…่Œ)
Risk Class 1

Registration Details

9f011a9a08e2bf446b4483ddcb28cbf4

DHA09600433807

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;; QMS/QSD

Dates and Status

Oct 15, 2020

Oct 15, 2025