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"Ekonti" Northby percutaneous cavity plasty balloon catheter - Taiwan Registration 1ed20af71ea4e8721b96d8385a5f4b44

Access comprehensive regulatory information for "Ekonti" Northby percutaneous cavity plasty 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 1ed20af71ea4e8721b96d8385a5f4b44 and manufactured by Acandis GmbH. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS CO., LTD..

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1ed20af71ea4e8721b96d8385a5f4b44
Registration Details
Taiwan FDA Registration: 1ed20af71ea4e8721b96d8385a5f4b44
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Device Details

"Ekonti" Northby percutaneous cavity plasty balloon catheter
TW: โ€œ่‰พๅบท่’‚โ€่ซพๆ–ฏๆฏ”็ถ“็šฎ็ฉฟ่…”ๆˆๅž‹่ก“ๆฐฃ็ƒๅฐŽ็ฎก
Risk Class 2

Registration Details

1ed20af71ea4e8721b96d8385a5f4b44

DHA05603070802

Company Information

Germany

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

Jan 17, 2018

Jan 17, 2028