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“Argon” Super Core Semi-Automatic Biopsy Instrument - Taiwan Registration 8a25e36205a98a6e9e7bc69063a930a3

Access comprehensive regulatory information for “Argon” Super Core Semi-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 8a25e36205a98a6e9e7bc69063a930a3 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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8a25e36205a98a6e9e7bc69063a930a3
Registration Details
Taiwan FDA Registration: 8a25e36205a98a6e9e7bc69063a930a3
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Device Details

“Argon” Super Core Semi-Automatic Biopsy Instrument
TW: “亞康恩”舒普克半自動組織切片器
Risk Class 2
MD

Registration Details

8a25e36205a98a6e9e7bc69063a930a3

Ministry of Health Medical Device Import No. 026771

DHA05602677107

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

Nov 04, 2014

Nov 04, 2024