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“Abbott” Armada 18 Percutaneous Transluminal Angioplasty (PTA) Catheter - Taiwan Registration fe95166b1b32a44ac4be7cd1e629ce4c

Access comprehensive regulatory information for “Abbott” Armada 18 Percutaneous Transluminal Angioplasty (PTA) Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe95166b1b32a44ac4be7cd1e629ce4c and manufactured by ABBOTT VASCULAR. The authorized representative in Taiwan is Abbott Medical Taiwan Co..

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fe95166b1b32a44ac4be7cd1e629ce4c
Registration Details
Taiwan FDA Registration: fe95166b1b32a44ac4be7cd1e629ce4c
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Device Details

“Abbott” Armada 18 Percutaneous Transluminal Angioplasty (PTA) Catheter
TW: “亞培”阿曼達18周邊血管球囊導管
Risk Class 2
MD

Registration Details

fe95166b1b32a44ac4be7cd1e629ce4c

Ministry of Health Medical Device Import No. 028147

DHA05602814709

Company Information

Ireland

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

Jan 15, 2016

Jan 15, 2026