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"Ambu" electronic bronchoscope and screen - Taiwan Registration 48a8170ffd3cac4ceeacf82efc78fa8c

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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48a8170ffd3cac4ceeacf82efc78fa8c
Registration Details
Taiwan FDA Registration: 48a8170ffd3cac4ceeacf82efc78fa8c
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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

48a8170ffd3cac4ceeacf82efc78fa8c

DHA05603275001

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

Contract manufacturing;; input

Dates and Status

Aug 03, 2019

Aug 03, 2024

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