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"Ginos" percutaneous puncture angioplasty balloon dilation catheter - Taiwan Registration b6c6b02fbf59a19ae7bc4f277e7107d5

Access comprehensive regulatory information for "Ginos" percutaneous puncture angioplasty 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 b6c6b02fbf59a19ae7bc4f277e7107d5 and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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b6c6b02fbf59a19ae7bc4f277e7107d5
Registration Details
Taiwan FDA Registration: b6c6b02fbf59a19ae7bc4f277e7107d5
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Device Details

"Ginos" percutaneous puncture angioplasty balloon dilation catheter
TW: โ€œๅ‰่ซพๅธโ€็ถ“็šฎ็ฉฟๅˆบ่ก€็ฎกๆˆๅฝข่ก“็ƒๅ›Šๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

b6c6b02fbf59a19ae7bc4f277e7107d5

DHA05603376707

Company Information

Korea, Republic of

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Jun 17, 2020

Jun 17, 2025