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"Covidien" Curiotracheal intubation - Taiwan Registration 78b87652b6f031e99fa0d7203733bc73

Access comprehensive regulatory information for "Covidien" Curiotracheal intubation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 78b87652b6f031e99fa0d7203733bc73 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.

This page provides complete technical specifications, regulatory compliance details. 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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78b87652b6f031e99fa0d7203733bc73
Registration Details
Taiwan FDA Registration: 78b87652b6f031e99fa0d7203733bc73
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Device Details

"Covidien" Curiotracheal intubation
TW: โ€œๆŸฏๆƒ โ€่ฌ้ˆ็ง‘้ฃŸ้“ๆฐฃ็ฎกๆ’็ฎก
Risk Class 2
Cancelled

Registration Details

78b87652b6f031e99fa0d7203733bc73

DHA00602012403

Company Information

Mexico;;United States

Product Details

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

D Anesthesiology

D.5650 Esophageal obstruction

import

Dates and Status

Aug 18, 2009

Aug 18, 2019

Mar 16, 2017

Cancellation Information

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