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"Ept" Konkel anchors balloon dilation catheter - Taiwan Registration 502bda2bc590a8ddc7b061b2bc172e05

Access comprehensive regulatory information for "Ept" Konkel anchors balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 502bda2bc590a8ddc7b061b2bc172e05 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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502bda2bc590a8ddc7b061b2bc172e05
Registration Details
Taiwan FDA Registration: 502bda2bc590a8ddc7b061b2bc172e05
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Device Details

"Ept" Konkel anchors balloon dilation catheter
TW: โ€œๅŸƒๆ™ฎ็‰นโ€ๅบทๅ…‹็ˆพ้Œจๅฎš็ƒๅ›Šๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

502bda2bc590a8ddc7b061b2bc172e05

DHA09200139409

Company Information

China

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

Chinese goods;; input

Dates and Status

Oct 23, 2022

Oct 23, 2027