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“BALTON”Fryderyk Coronary Angioplasty Catheter - Taiwan Registration 1fd7cbb7c199d705fe674aa2767630be

Access comprehensive regulatory information for “BALTON”Fryderyk Coronary Angioplasty Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fd7cbb7c199d705fe674aa2767630be and manufactured by Balton Sp.z o.o.. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..

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1fd7cbb7c199d705fe674aa2767630be
Registration Details
Taiwan FDA Registration: 1fd7cbb7c199d705fe674aa2767630be
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Device Details

“BALTON”Fryderyk Coronary Angioplasty Catheter
TW: “拜登”腓特烈冠狀動脈成形術導管
Risk Class 2
MD

Registration Details

1fd7cbb7c199d705fe674aa2767630be

Ministry of Health Medical Device Import No. 035409

DHA05603540904

Company Information

Poland

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E0005 Percutaneous puncture of the coronary ductus

Imported from abroad

Dates and Status

Apr 17, 2022

Apr 17, 2027