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"Covidien" endoscopic surgical instruments - Taiwan Registration 728b7877f42399e24e247dd6bdbadcb9

Access comprehensive regulatory information for "Covidien" endoscopic surgical instruments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 728b7877f42399e24e247dd6bdbadcb9 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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728b7877f42399e24e247dd6bdbadcb9
Registration Details
Taiwan FDA Registration: 728b7877f42399e24e247dd6bdbadcb9
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Device Details

"Covidien" endoscopic surgical instruments
TW: โ€œๆŸฏๆƒ โ€ๅ…ง่ฆ–้กๆ‰‹่ก“ๅ™จๆขฐ
Risk Class 2

Registration Details

728b7877f42399e24e247dd6bdbadcb9

DHA05603301907

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

Dec 08, 2019

Dec 08, 2029

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