Taiwan FDA registration caa66f938740ea9f6a4160976c9a57f2

"Abbott" Fox small blood vessel peripheral vascular balloon catheter

TW: “亞培”福克斯小血管周邊血管氣球導管
Taiwan flagTaiwan·Risk Class 2·ABBOTT LABORATORIES VASCULAR ENTERPRISES LIMITED, DUBLIN, BERINGEN BRANCH·Registered May 12, 2010 – May 12, 2020Cancelled
Registration details
Analysis ID
caa66f938740ea9f6a4160976c9a57f2
Customs Code
DHA00602102009
Company information
Manufacturer Country
Switzerland
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1250 Percutaneous catheters
Import Information
import
Dates and status
Registration Date
May 12, 2010
Expiry Date
May 12, 2020
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for "Abbott" Fox small blood vessel peripheral vascular balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number caa66f938740ea9f6a4160976c9a57f2 and manufactured by ABBOTT LABORATORIES VASCULAR ENTERPRISES LIMITED, DUBLIN, BERINGEN BRANCH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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