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"Covidien" endoscopic automatic vascular clamp - Taiwan Registration 7133a00d33cf5ea27a11c4a5d2b8680f

Access comprehensive regulatory information for "Covidien" endoscopic automatic vascular clamp in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7133a00d33cf5ea27a11c4a5d2b8680f and manufactured by COVIDIEN LLC;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including COVIDIEN LLC;; COVID, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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7133a00d33cf5ea27a11c4a5d2b8680f
Registration Details
Taiwan FDA Registration: 7133a00d33cf5ea27a11c4a5d2b8680f
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Device Details

"Covidien" endoscopic automatic vascular clamp
TW: "ๆŸฏๆƒ " ๅ…ง่ฆ–้ก่‡ชๅ‹•่ก€็ฎกๅคพ
Risk Class 2

Registration Details

7133a00d33cf5ea27a11c4a5d2b8680f

DHA00601073500

Company Information

Dominican Republic;;United States

Product Details

I General, Plastic Surgery and Dermatology

import

Dates and Status

Jun 30, 2004

Jun 30, 2029

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