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"Tampa" single-use double-lumen bronchial intubation - Taiwan Registration 4ac75467b393a675cc055173efd34596

Access comprehensive regulatory information for "Tampa" single-use double-lumen bronchial intubation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ac75467b393a675cc055173efd34596 and manufactured by Hangzhou Tappa Medical Technology Co., Ltd.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE 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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4ac75467b393a675cc055173efd34596
Registration Details
Taiwan FDA Registration: 4ac75467b393a675cc055173efd34596
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Device Details

"Tampa" single-use double-lumen bronchial intubation
TW: โ€œๅฆๅธ•โ€ไธ€ๆฌกๆ€งไฝฟ็”จ้›™่…”ๆ”ฏๆฐฃ็ฎกๆ’็ฎก
Risk Class 2

Registration Details

4ac75467b393a675cc055173efd34596

DHA09200106503

Company Information

Product Details

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

D Anesthesiology

D.5720 Bronchi inner pipe

Chinese goods;; input

Dates and Status

Sep 09, 2019

Sep 09, 2024