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"Apricot Whole" blood lancet (sterilized) - Taiwan Registration 203f338f0aef01d6d32075419f71f87a

Access comprehensive regulatory information for "Apricot Whole" 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 203f338f0aef01d6d32075419f71f87a and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL 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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203f338f0aef01d6d32075419f71f87a
Registration Details
Taiwan FDA Registration: 203f338f0aef01d6d32075419f71f87a
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Device Details

"Apricot Whole" blood lancet (sterilized)
TW: "ๆๅ…จ" ๆŽก่ก€้‡ (ๆป…่Œ)
Risk Class 1

Registration Details

203f338f0aef01d6d32075419f71f87a

DHA04600181701

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

QMS/QSD;; Input;; Chinese goods

Dates and Status

Jan 03, 2013

Jan 03, 2023