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"Dayan" bronchial atresia catheter - Taiwan Registration 8e3d71c6ed84ff99da2aa1ad76a9ad36

Access comprehensive regulatory information for "Dayan" 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 8e3d71c6ed84ff99da2aa1ad76a9ad36 and manufactured by DAIKEN MEDICAL CO., LTD.. The authorized representative in Taiwan is YUAN MIN ENTERPRISE CO., LTD..

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8e3d71c6ed84ff99da2aa1ad76a9ad36
Registration Details
Taiwan FDA Registration: 8e3d71c6ed84ff99da2aa1ad76a9ad36
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Device Details

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

Registration Details

8e3d71c6ed84ff99da2aa1ad76a9ad36

DHA00601849507

Company Information

Japan

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

Oct 09, 2012

Dec 12, 2027