Taiwan FDA registration 28919feda3cccae26ab8f98da4618c47

"Ambu" electronic bronchoscope and screen

TW: “安佈”電子式支氣管鏡及螢幕
Taiwan flagTaiwan·Risk Class 2·AMBU SDN BHD;; AMBU A/S·Registered Jun 06, 2017 – Jun 06, 2027Active
Registration details
Analysis ID
28919feda3cccae26ab8f98da4618c47
Customs Code
DHA05602988804
Company information
Manufacturer Country
Malaysia;;Denmark
Authorized Representative
HWA YI MEDICAL CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
G ENT Science
Product Type (Level 2)
G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Jun 06, 2017
Expiry Date
Jun 06, 2027
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About this record

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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