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"Weiren" blood lancet (sterilized) - Taiwan Registration 5afcc00acd31ef4ebd79d27827112f1a

Access comprehensive regulatory information for "Weiren" blood lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5afcc00acd31ef4ebd79d27827112f1a and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is WELLAN TECH CO., LTD..

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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5afcc00acd31ef4ebd79d27827112f1a
Registration Details
Taiwan FDA Registration: 5afcc00acd31ef4ebd79d27827112f1a
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Device Details

"Weiren" blood lancet (sterilized)
TW: "ๅ‰ไปป" ๆŽก่ก€้‡ (ๆป…่Œ)
Risk Class 1

Registration Details

5afcc00acd31ef4ebd79d27827112f1a

DHA09600347308

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;; Chinese goods

Dates and Status

Jul 02, 2018

Jul 02, 2028