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"Lepu" amber percutaneous puncture coronary balloon catheter - Taiwan Registration 9bc104759fa8cef0c7d9ad3201b00a13

Access comprehensive regulatory information for "Lepu" amber percutaneous puncture coronary balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9bc104759fa8cef0c7d9ad3201b00a13 and manufactured by Lepu Medical Technology (Beijing) Co., Ltd.. The authorized representative in Taiwan is SUNNY HEART SCIENTIFIC 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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9bc104759fa8cef0c7d9ad3201b00a13
Registration Details
Taiwan FDA Registration: 9bc104759fa8cef0c7d9ad3201b00a13
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Device Details

"Lepu" amber percutaneous puncture coronary balloon catheter
TW: โ€œๆจ‚ๆ™ฎโ€็ฅ็€็ถ“็šฎ็ฉฟๅˆบๅ† ็‹€ๅ‹•่„ˆ็ƒๅ›ŠๅฐŽ็ฎก
Risk Class 3
Cancelled

Registration Details

9bc104759fa8cef0c7d9ad3201b00a13

DHA09200058702

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.0005.

Chinese goods;; input

Dates and Status

Apr 25, 2014

Apr 25, 2019

Jun 16, 2022

Cancellation Information

Logged out

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