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"Fusch" bronchial atresia catheter - Taiwan Registration f32e5183dc2ec4cc0293e9fb49f8b3fd

Access comprehensive regulatory information for "Fusch" bronchial 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 f32e5183dc2ec4cc0293e9fb49f8b3fd and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..

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f32e5183dc2ec4cc0293e9fb49f8b3fd
Registration Details
Taiwan FDA Registration: f32e5183dc2ec4cc0293e9fb49f8b3fd
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Device Details

"Fusch" bronchial atresia catheter
TW: โ€œๅฏŒไธ–โ€ๆ”ฏๆฐฃ็ฎก้–‰้Ž–ๅฐŽ็ฎก
Risk Class 2

Registration Details

f32e5183dc2ec4cc0293e9fb49f8b3fd

DHA00602447704

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

Feb 21, 2013

Feb 21, 2023