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"Esme" ureteroscopy - Taiwan Registration a3fd07709f9d33c1b842801304e35ce3

Access comprehensive regulatory information for "Esme" ureteroscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a3fd07709f9d33c1b842801304e35ce3 and manufactured by GYRUS ACMI Inc.. The authorized representative in Taiwan is SHARPMED INSTRUMENTS 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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a3fd07709f9d33c1b842801304e35ce3
Registration Details
Taiwan FDA Registration: a3fd07709f9d33c1b842801304e35ce3
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Device Details

"Esme" ureteroscopy
TW: "่‰พๆ–ฏ็พŽ" ่ผธๅฐฟ็ฎก้ก
Risk Class 2
Cancelled

Registration Details

a3fd07709f9d33c1b842801304e35ce3

DHA00601262809

Company Information

United States

Product Details

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

H Gastroenterology and urology

import

Dates and Status

Oct 07, 2005

Oct 07, 2015

Apr 25, 2018

Cancellation Information

Logged out

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