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"Covidien" laparoscopic puncture cannula holder - Taiwan Registration f392c1e3a29a3093332e6e844eb1e8f7

Access comprehensive regulatory information for "Covidien" laparoscopic puncture cannula holder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f392c1e3a29a3093332e6e844eb1e8f7 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;; Covidien, 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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f392c1e3a29a3093332e6e844eb1e8f7
Registration Details
Taiwan FDA Registration: f392c1e3a29a3093332e6e844eb1e8f7
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Device Details

"Covidien" laparoscopic puncture cannula holder
TW: โ€œๆŸฏๆƒ โ€่…น่…”้ก็ฉฟๅˆบๅฅ—็ฎกๅ›บๅฎšๅ™จ
Risk Class 2
Cancelled

Registration Details

f392c1e3a29a3093332e6e844eb1e8f7

DHA00602517404

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

Jul 09, 2013

Jul 09, 2018

Jun 16, 2022

Cancellation Information

Logged out

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