“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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Device Details
Registration Details
fe95166b1b32a44ac4be7cd1e629ce4c
Ministry of Health Medical Device Import No. 028147
DHA05602814709
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

