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"Henan camel man" double-lumen bronchial atresia catheter - Taiwan Registration 64e79a81f4589df86bf454926499a7d4

Access comprehensive regulatory information for "Henan camel man" double-lumen bronchial atresia catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 64e79a81f4589df86bf454926499a7d4 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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64e79a81f4589df86bf454926499a7d4
Registration Details
Taiwan FDA Registration: 64e79a81f4589df86bf454926499a7d4
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Device Details

"Henan camel man" double-lumen bronchial atresia catheter
TW: โ€œๆฒณๅ—้งไบบโ€้›™่…”ๆ”ฏๆฐฃ็ฎก้–‰้Ž–ๅฐŽ็ฎก
Risk Class 2

Registration Details

64e79a81f4589df86bf454926499a7d4

DHA09200080502

Company Information

Product Details

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

D Anesthesiology

D.5740 Gas pipe/bronchi divergence gas line

Input;; Chinese goods

Dates and Status

Dec 22, 2016

Dec 22, 2026