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"Covidien" V-blade puncture sleeve - Taiwan Registration c5a1921757605055fc6d84355ddb63b6

Access comprehensive regulatory information for "Covidien" V-blade puncture sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5a1921757605055fc6d84355ddb63b6 and manufactured by COVIDIEN LLC;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including COVIDIEN LLC;; Covidien, COVIDIEN LLC;; COVID, and 4 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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c5a1921757605055fc6d84355ddb63b6
Registration Details
Taiwan FDA Registration: c5a1921757605055fc6d84355ddb63b6
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Device Details

"Covidien" V-blade puncture sleeve
TW: "ๆŸฏๆƒ " Vๅž‹ๅˆ€็‰‡็ฉฟๅˆบๅฅ—็ฎก
Risk Class 2

Registration Details

c5a1921757605055fc6d84355ddb63b6

DHA00601365201

Company Information

Dominican Republic;;United States

Product Details

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

H Gastroenterology and urology

Contract manufacturing;; input

Dates and Status

Nov 23, 2005

Nov 23, 2025

Nov 06, 2024

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