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"Amber" Mark Awakener - Taiwan Registration 69aeae737957bf6127a0b4c1aaeda9a8

Access comprehensive regulatory information for "Amber" Mark Awakener in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 69aeae737957bf6127a0b4c1aaeda9a8 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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69aeae737957bf6127a0b4c1aaeda9a8
Registration Details
Taiwan FDA Registration: 69aeae737957bf6127a0b4c1aaeda9a8
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Device Details

"Amber" Mark Awakener
TW: โ€œๅฎ‰ๅฏถโ€้ฆฌๅ…‹็”ฆ้†’ๅ™จ
Risk Class 2
Cancelled

Registration Details

69aeae737957bf6127a0b4c1aaeda9a8

DHA04200038701

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;; Contract manufacturing

Dates and Status

Sep 22, 2011

Sep 22, 2016

Jun 25, 2018

Cancellation Information

Logged out

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