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"Xianjian" vena cava filter - Taiwan Registration 0d79cbe344f1f7214118b332d38bc904

Access comprehensive regulatory information for "Xianjian" vena cava filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0d79cbe344f1f7214118b332d38bc904 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is SHIUH-CHYNG MEDICAL CO., 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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0d79cbe344f1f7214118b332d38bc904
Registration Details
Taiwan FDA Registration: 0d79cbe344f1f7214118b332d38bc904
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Device Details

"Xianjian" vena cava filter
TW: โ€œๅ…ˆๅฅโ€่…”้œ่„ˆ้Žๆฟพๅ™จ
Risk Class 2
Cancelled

Registration Details

0d79cbe344f1f7214118b332d38bc904

DHA04200032202

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.4260 Cardiopulmonary vascular bypass artery blood spiller

Chinese goods;; input

Dates and Status

Dec 21, 2011

Dec 21, 2016

Aug 14, 2018

Cancellation Information

Logged out

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