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“DA CHUNG” Manual Resuscitator Kit and Accessory - Taiwan Registration ab853721fff270c4894932b52025fecf

Access comprehensive regulatory information for “DA CHUNG” Manual Resuscitator Kit and Accessory in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab853721fff270c4894932b52025fecf and manufactured by DA CHUNG MEDICAL CO., LTD.. The authorized representative in Taiwan is DA CHUNG MEDICAL CO., LTD..

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Registration Details
Taiwan FDA Registration: ab853721fff270c4894932b52025fecf
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Device Details

“DA CHUNG” Manual Resuscitator Kit and Accessory
TW: “大中”甦醒球組及其零配件
Risk Class 2
MD
Cancelled

Registration Details

ab853721fff270c4894932b52025fecf

Ministry of Health Medical Device Manufacturing No. 004296

Company Information

Taiwan, Province of China

Product Details

D Devices for anesthesiology

D5915 Manual Emergency Respirator

Produced in Taiwan, China

Dates and Status

Nov 28, 2013

Nov 28, 2018

Jul 15, 2022

Cancellation Information

Logged out

未展延而逾期者