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"Ambu" electronic bronchoscope and screen - Taiwan Registration 28919feda3cccae26ab8f98da4618c47

Access comprehensive regulatory information for "Ambu" electronic bronchoscope and screen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 28919feda3cccae26ab8f98da4618c47 and manufactured by AMBU SDN BHD;; AMBU A/S. The authorized representative in Taiwan is HWA YI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Ambu Sdn. Bhd.;; AMBU A/S, and 1 recent registrations in the same category. 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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28919feda3cccae26ab8f98da4618c47
Registration Details
Taiwan FDA Registration: 28919feda3cccae26ab8f98da4618c47
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Device Details

"Ambu" electronic bronchoscope and screen
TW: โ€œๅฎ‰ไฝˆโ€้›ปๅญๅผๆ”ฏๆฐฃ็ฎก้กๅŠ่žขๅน•
Risk Class 2

Registration Details

28919feda3cccae26ab8f98da4618c47

DHA05602988804

Company Information

Malaysia;;Denmark

Product Details

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

G ENT Science

G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof

Input;; Contract manufacturing

Dates and Status

Jun 06, 2017

Jun 06, 2027

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