Taiwan FDA registration 48a8170ffd3cac4ceeacf82efc78fa8c

"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 Aug 03, 2019 – Aug 03, 2024Expired
Registration details
Analysis ID
48a8170ffd3cac4ceeacf82efc78fa8c
Customs Code
DHA05603275001
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
Contract manufacturing;; input
Dates and status
Registration Date
Aug 03, 2019
Expiry Date
Aug 03, 2024
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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 48a8170ffd3cac4ceeacf82efc78fa8c 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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