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“Medtronic” CELLO balloon guide catheter - Taiwan Registration b45ce90abb327777bbf53fd5a1c210a2

Access comprehensive regulatory information for “Medtronic” CELLO balloon guide catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b45ce90abb327777bbf53fd5a1c210a2 and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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b45ce90abb327777bbf53fd5a1c210a2
Registration Details
Taiwan FDA Registration: b45ce90abb327777bbf53fd5a1c210a2
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Device Details

“Medtronic” CELLO balloon guide catheter
TW: “美敦力”協樂球囊導引導管
Risk Class 2
MD

Registration Details

b45ce90abb327777bbf53fd5a1c210a2

Ministry of Health Medical Device Import No. 028523

DHA05602852301

Company Information

Product Details

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

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

May 02, 2016

May 02, 2026