Taiwan FDA registration fe95166b1b32a44ac4be7cd1e629ce4c
“Abbott” Armada 18 Percutaneous Transluminal Angioplasty (PTA) Catheter
TW: “亞培”阿曼達18周邊血管球囊導管
Taiwan·Risk Class 2·MD·ABBOTT VASCULAR·Registered Jan 15, 2016 – Jan 15, 2026ExpiredRegistration details
- Analysis ID
- fe95166b1b32a44ac4be7cd1e629ce4c
- License Form
- Ministry of Health Medical Device Import No. 028147
- Customs Code
- DHA05602814709
Company information
- Manufacturer
- ABBOTT VASCULAR
- Manufacturer Country
- Ireland
- Authorized Representative
- Abbott Medical Taiwan Co.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 15, 2016
- Expiry Date
- Jan 15, 2026
About this record
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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