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“Argon” Tru-Core II Automatic Biopsy Instrument - Taiwan Registration 6acec88b61570e3c428f1fb35a266c70

Access comprehensive regulatory information for “Argon” Tru-Core II 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 6acec88b61570e3c428f1fb35a266c70 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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6acec88b61570e3c428f1fb35a266c70
Registration Details
Taiwan FDA Registration: 6acec88b61570e3c428f1fb35a266c70
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Device Details

“Argon” Tru-Core II Automatic Biopsy Instrument
TW: “亞康恩”楚克自動組織切片器
Risk Class 2
MD

Registration Details

6acec88b61570e3c428f1fb35a266c70

Ministry of Health Medical Device Import No. 026885

DHA05602688509

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

Dec 27, 2014

Dec 27, 2024