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"Covidien" Vivienco Sherry Extended Pneumatic Cannula - Taiwan Registration de8c20bc07ba61d359edf7d52138b10c

Access comprehensive regulatory information for "Covidien" Vivienco Sherry Extended Pneumatic Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number de8c20bc07ba61d359edf7d52138b10c and manufactured by COVIDIEN LLC;; MALLINCKRODT MEDICAL. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including COVIDIEN LLC;; MALLINCKRODT MEDICAL, 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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de8c20bc07ba61d359edf7d52138b10c
Registration Details
Taiwan FDA Registration: de8c20bc07ba61d359edf7d52138b10c
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Device Details

"Covidien" Vivienco Sherry Extended Pneumatic Cannula
TW: "ๆŸฏๆƒ "่ฌ้ˆ็ง‘้›ช่މๅŠ ้•ทๅž‹ๆฐฃๅˆ‡ๅฅ—็ฎก
Risk Class 2
Cancelled

Registration Details

de8c20bc07ba61d359edf7d52138b10c

DHA00601858202

Company Information

Ireland;;United States

Product Details

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

D Anesthesiology

import

Dates and Status

Feb 04, 2008

Feb 04, 2018

Mar 16, 2017

Cancellation Information

Logged out

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