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"Abbott" Foss deep peripheral vascular balloon catheter - Taiwan Registration 79fbe17368e5504341a0f71ee3b5721b

Access comprehensive regulatory information for "Abbott" Foss deep 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 79fbe17368e5504341a0f71ee3b5721b and manufactured by ABBOTT LABORATORIES VASCULAR ENTERPRISES LIMITED, DUBLIN, BERINGEN BRANCH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..

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79fbe17368e5504341a0f71ee3b5721b
Registration Details
Taiwan FDA Registration: 79fbe17368e5504341a0f71ee3b5721b
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Device Details

"Abbott" Foss deep peripheral vascular balloon catheter
TW: โ€œไบžๅŸนโ€็ฆๆ–ฏๆทฑๅฑคๅ‘จ้‚Š่ก€็ฎกๆฐฃ็ƒๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

79fbe17368e5504341a0f71ee3b5721b

DHA00601838003

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

Oct 29, 2007

Oct 29, 2012

Mar 27, 2014

Cancellation Information

Logged out

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