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“Argon” Pro-Mag Ultra Automatic Biopsy Instrument - Taiwan Registration c4f1b15e406363a3e9505b47771258c4

Access comprehensive regulatory information for “Argon” Pro-Mag Ultra Automatic Biopsy Instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c4f1b15e406363a3e9505b47771258c4 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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c4f1b15e406363a3e9505b47771258c4
Registration Details
Taiwan FDA Registration: c4f1b15e406363a3e9505b47771258c4
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Device Details

“Argon” Pro-Mag Ultra Automatic Biopsy Instrument
TW: “亞康恩”剖美克全自動組織切片器
Risk Class 2
MD

Registration Details

c4f1b15e406363a3e9505b47771258c4

Ministry of Health Medical Device Import No. 026897

DHA05602689703

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

Jan 05, 2015

Jan 05, 2025