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"Covidien" V-blade puncture sleeve - Taiwan Registration d691013a796e392d188be3d7d9fd9c7a

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 d691013a796e392d188be3d7d9fd9c7a and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.

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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d691013a796e392d188be3d7d9fd9c7a
Registration Details
Taiwan FDA Registration: d691013a796e392d188be3d7d9fd9c7a
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Device Details

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

Registration Details

d691013a796e392d188be3d7d9fd9c7a

DHA00602494906

Company Information

United States

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

May 07, 2013

May 07, 2018

Mar 16, 2017

Cancellation Information

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