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"Covidien" Viviencoe endotracheal tube - Taiwan Registration 53b8b574651dd80783c4c507c3211a08

Access comprehensive regulatory information for "Covidien" Viviencoe endotracheal tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 53b8b574651dd80783c4c507c3211a08 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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53b8b574651dd80783c4c507c3211a08
Registration Details
Taiwan FDA Registration: 53b8b574651dd80783c4c507c3211a08
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Device Details

"Covidien" Viviencoe endotracheal tube
TW: "ๆŸฏๆƒ "่ฌ้ˆ็ง‘ๆฐฃ็ฎกๅ…ง็ฎก
Risk Class 2
Cancelled

Registration Details

53b8b574651dd80783c4c507c3211a08

DHA00602065600

Company Information

Ireland;;United States

Product Details

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

D Anesthesiology

D.5730 Endotracheal tubes

import

Dates and Status

Mar 12, 2010

Mar 12, 2020

Mar 16, 2017

Cancellation Information

Logged out

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