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"Fushi" bronchial tube blocker - Taiwan Registration 7def660d2e4c047d803cc4ea4a13aca9

Access comprehensive regulatory information for "Fushi" bronchial tube blocker in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7def660d2e4c047d803cc4ea4a13aca9 and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..

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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7def660d2e4c047d803cc4ea4a13aca9
Registration Details
Taiwan FDA Registration: 7def660d2e4c047d803cc4ea4a13aca9
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Device Details

"Fushi" bronchial tube blocker
TW: โ€œๅฏŒไธ–โ€ๆ”ฏๆฐฃ็ฎกๅ…ง็ฎก้˜ป้š”ๅ™จ
Risk Class 2

Registration Details

7def660d2e4c047d803cc4ea4a13aca9

DHA00602448006

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 25, 2013

Feb 25, 2028