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"Apt" Zurich guide line - Taiwan Registration 0a19e64024cdce2e581b7ac9e73061db

Access comprehensive regulatory information for "Apt" Zurich guide line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a19e64024cdce2e581b7ac9e73061db and manufactured by APT Medical Inc.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY 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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0a19e64024cdce2e581b7ac9e73061db
Registration Details
Taiwan FDA Registration: 0a19e64024cdce2e581b7ac9e73061db
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Device Details

"Apt" Zurich guide line
TW: โ€œๅŸƒๆ™ฎ็‰นโ€่˜‡้ปŽไธ–ๅฐŽๅผ•็ทš
Risk Class 2

Registration Details

0a19e64024cdce2e581b7ac9e73061db

DHA09200133302

Company Information

China

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1330 Catheter Guide Wires

Input;; Chinese goods

Dates and Status

Apr 23, 2022

Apr 23, 2027