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"Ambao" Oufu Prastrass Awakener - Taiwan Registration 64959a159d75db18417883bf74b75311

Access comprehensive regulatory information for "Ambao" Oufu Prastrass Awakener in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 64959a159d75db18417883bf74b75311 and manufactured by AMBU A/S;; AMBU LTD.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., 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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64959a159d75db18417883bf74b75311
Registration Details
Taiwan FDA Registration: 64959a159d75db18417883bf74b75311
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Device Details

"Ambao" Oufu Prastrass Awakener
TW: โ€œๅฎ‰ๅฏถโ€ๆญ่ผ”ๆ™ฎๆ‹‰ๅธ็”ฆ้†’ๅ™จ
Risk Class 2
Cancelled

Registration Details

64959a159d75db18417883bf74b75311

DHA04200043502

Company Information

Denmark;;China

Product Details

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

D Anesthesiology

D.5915 Hand emergency breathing apparatus

Input;; Chinese goods

Dates and Status

Jul 16, 2012

Jul 16, 2017

Dec 20, 2019

Cancellation Information

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