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"Ambo" Oufu awakener - Taiwan Registration 4f5f641f1524f0b2a46d51df82c3cec7

Access comprehensive regulatory information for "Ambo" Oufu awakener in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4f5f641f1524f0b2a46d51df82c3cec7 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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4f5f641f1524f0b2a46d51df82c3cec7
Registration Details
Taiwan FDA Registration: 4f5f641f1524f0b2a46d51df82c3cec7
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Device Details

"Ambo" Oufu awakener
TW: โ€œๅฎ‰ๅฏถโ€ๆญ่ผ”็”ฆ้†’ๅ™จ
Risk Class 2
Cancelled

Registration Details

4f5f641f1524f0b2a46d51df82c3cec7

DHA04200043400

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

Contract manufacturing;; input

Dates and Status

Jul 16, 2012

Jul 16, 2017

Dec 20, 2019

Cancellation Information

Logged out

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