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"Fuji" Serbronchial atresia catheter - Taiwan Registration 1dc7359e5f22f701ac1964f48f9d9303

Access comprehensive regulatory information for "Fuji" Serbronchial atresia catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1dc7359e5f22f701ac1964f48f9d9303 and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..

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1dc7359e5f22f701ac1964f48f9d9303
Registration Details
Taiwan FDA Registration: 1dc7359e5f22f701ac1964f48f9d9303
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Device Details

"Fuji" Serbronchial atresia catheter
TW: โ€œๅฏŒๅฃซโ€ๅกž็ˆพๅธƒๆœ—ๆ”ฏๆฐฃ็ฎก้–‰้Ž–ๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

1dc7359e5f22f701ac1964f48f9d9303

DHA00602439005

Company Information

Product Details

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

D Anesthesiology

D.5740 Gas pipe/bronchi divergence gas line

import

Dates and Status

Jan 09, 2013

Jan 09, 2018

Dec 13, 2019

Cancellation Information

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