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“Gyrus ACMI” Adjustable Biopsy Port Seal Y-Adapter - Taiwan Registration 3a0ed46112d521b3c3b3246217c3fa08

Access comprehensive regulatory information for “Gyrus ACMI” Adjustable Biopsy Port Seal Y-Adapter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3a0ed46112d521b3c3b3246217c3fa08 and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT 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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3a0ed46112d521b3c3b3246217c3fa08
Registration Details
Taiwan FDA Registration: 3a0ed46112d521b3c3b3246217c3fa08
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Device Details

“Gyrus ACMI” Adjustable Biopsy Port Seal Y-Adapter
TW: “吉洛氏 艾斯米”可調式穿刺Y形轉接頭
Risk Class 2
MD

Registration Details

3a0ed46112d521b3c3b3246217c3fa08

Ministry of Health Medical Device Import No. 026877

DHA05602687700

Company Information

United States

Product Details

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

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Dec 25, 2014

Dec 25, 2024