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“Tru-Core” I Biopsy Needles - Taiwan Registration b21c5cc485322afdcd6614808801ab97

Access comprehensive regulatory information for “Tru-Core” I Biopsy Needles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b21c5cc485322afdcd6614808801ab97 and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is CHINA SPRING TRADING 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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b21c5cc485322afdcd6614808801ab97
Registration Details
Taiwan FDA Registration: b21c5cc485322afdcd6614808801ab97
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Device Details

“Tru-Core” I Biopsy Needles
TW: “楚克”切片針
Risk Class 2
MD

Registration Details

b21c5cc485322afdcd6614808801ab97

Ministry of Health Medical Device Import No. 025507

DHA05602550701

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology-urology devices

H1075 Gastroenterology - Urology biopsy instruments

Imported from abroad

Dates and Status

Oct 24, 2013

Oct 24, 2023