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"AXA" blood lancet (sterilized) - Taiwan Registration fda8c638450720c6384002eb9947e802

Access comprehensive regulatory information for "AXA" 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 fda8c638450720c6384002eb9947e802 and manufactured by TIANJIN HUAHONG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is IXENSOR 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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fda8c638450720c6384002eb9947e802
Registration Details
Taiwan FDA Registration: fda8c638450720c6384002eb9947e802
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Device Details

"AXA" blood lancet (sterilized)
TW: "ๅฎ‰็››" ๆŽก่ก€้‡(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

fda8c638450720c6384002eb9947e802

DHA09600253907

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

Input;; Chinese goods;; QMS/QSD

Dates and Status

Nov 02, 2015

Nov 02, 2020

Jul 15, 2022

Cancellation Information

Logged out

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