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"Abbott" Fox small blood vessel peripheral vascular balloon catheter - Taiwan Registration caa66f938740ea9f6a4160976c9a57f2

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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caa66f938740ea9f6a4160976c9a57f2
Registration Details
Taiwan FDA Registration: caa66f938740ea9f6a4160976c9a57f2
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Device Details

"Abbott" Fox small blood vessel peripheral vascular balloon catheter
TW: โ€œไบžๅŸนโ€็ฆๅ…‹ๆ–ฏๅฐ่ก€็ฎกๅ‘จ้‚Š่ก€็ฎกๆฐฃ็ƒๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

caa66f938740ea9f6a4160976c9a57f2

DHA00602102009

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

May 12, 2010

May 12, 2020

Jul 15, 2022

Cancellation Information

Logged out

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