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“Henan Tuoren” Endotracheal Tube - Taiwan Registration b75c6552ccaf2e68d6a7a7d69a0c15b5

Access comprehensive regulatory information for “Henan Tuoren” Endotracheal Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b75c6552ccaf2e68d6a7a7d69a0c15b5 and manufactured by HENAN TUOREN MEDICAL DEVICE 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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b75c6552ccaf2e68d6a7a7d69a0c15b5
Registration Details
Taiwan FDA Registration: b75c6552ccaf2e68d6a7a7d69a0c15b5
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Device Details

“Henan Tuoren” Endotracheal Tube
TW: “河南駝人” 氣管內管
Risk Class 2
MD

Registration Details

b75c6552ccaf2e68d6a7a7d69a0c15b5

Ministry of Health Medical Device Land Transport No. 000964

DHA09200096406

Company Information

Product Details

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

D Devices for anesthesiology

D5730 Endotracheal tube

Imported from abroad; Made in China

Dates and Status

Dec 11, 2018

Dec 11, 2028