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"Covidien" endoscopic automatic vascular clamp - Taiwan Registration b2817ebcb52ffc8b03ebf6f9b8e332a7

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 b2817ebcb52ffc8b03ebf6f9b8e332a7 and manufactured by COVIDIEN LLC;; COVID. 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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b2817ebcb52ffc8b03ebf6f9b8e332a7
Registration Details
Taiwan FDA Registration: b2817ebcb52ffc8b03ebf6f9b8e332a7
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Device Details

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

Registration Details

b2817ebcb52ffc8b03ebf6f9b8e332a7

DHA00602445902

Company Information

United States

Product Details

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

I General, Plastic Surgery and Dermatology

I.4300 Implantable Clips

import

Dates and Status

Jan 21, 2013

Jan 21, 2018

Dec 13, 2019

Cancellation Information

Logged out

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