Taiwan FDA registration 2aa7d76fd772b0898a320a24de308a66
"Abbott" Puxdale Percutaneous Vascular Suture & Prosthetic System
TW: “雅培” 普克斯戴爾經皮血管縫合與修復器系統
Taiwan·Risk Class 3·ABBOTT VASCULAR·Registered Feb 24, 2022 – Feb 24, 2027ActiveRegistration details
- Analysis ID
- 2aa7d76fd772b0898a320a24de308a66
- Customs Code
- DHA05603531406
Company information
- Manufacturer
- ABBOTT VASCULAR
- Manufacturer Country
- Ireland
- Authorized Representative
- Abbott Medical Taiwan Co.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 經皮導管;; E.9999 其他
- Import Information
- import
Dates and status
- Registration Date
- Feb 24, 2022
- Expiry Date
- Feb 24, 2027
About this record
Access comprehensive regulatory information for "Abbott" Puxdale Percutaneous Vascular Suture & Prosthetic System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2aa7d76fd772b0898a320a24de308a66 and manufactured by ABBOTT VASCULAR. The authorized representative in Taiwan is Abbott Medical Taiwan Co..
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