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"Xingchang" blood circuit tube - Taiwan Registration 14f725547492cd6b22c25b31a209ba46

Access comprehensive regulatory information for "Xingchang" blood circuit tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14f725547492cd6b22c25b31a209ba46 and manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.. The authorized representative in Taiwan is HI-CLEARANCE INC..

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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14f725547492cd6b22c25b31a209ba46
Registration Details
Taiwan FDA Registration: 14f725547492cd6b22c25b31a209ba46
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Device Details

"Xingchang" blood circuit tube
TW: โ€œๆๆ˜Œโ€่ก€ๆถฒ่ฟด่ทฏ็ฎก
Risk Class 2

Registration Details

14f725547492cd6b22c25b31a209ba46

DHA04200043907

Company Information

Product Details

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

H Gastroenterology and urology

H.5540 Blood Access Devices and Accessories

Chinese goods;; input

Dates and Status

Apr 26, 2012

Apr 26, 2027