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"Serucun" percutaneous intravascular angioplasty balloon catheter - Taiwan Registration 5a2717752125261b6da2b78d00f79d5e

Access comprehensive regulatory information for "Serucun" percutaneous intravascular angioplasty balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a2717752125261b6da2b78d00f79d5e and manufactured by M.A. Med Alliance SA;; MedAlliance LLC. The authorized representative in Taiwan is REGISTAR CO., LTD..

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5a2717752125261b6da2b78d00f79d5e
Registration Details
Taiwan FDA Registration: 5a2717752125261b6da2b78d00f79d5e
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Device Details

"Serucun" percutaneous intravascular angioplasty balloon catheter
TW: โ€œ็‘Ÿ็’ๆฝฏโ€็ถ“็šฎ่ก€็ฎกๅ…ง่ก€็ฎกๆˆๅฝข่ก“็ƒๅ›ŠๅฐŽ็ฎก
Risk Class 2

Registration Details

5a2717752125261b6da2b78d00f79d5e

DHA05603599504

Company Information

United States;;Switzerland

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Feb 21, 2023

Feb 21, 2028