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"Xingchang" plasma filtration waste bag (unsterilized) - Taiwan Registration 634d52224fd056c9273264277824afc2

Access comprehensive regulatory information for "Xingchang" plasma filtration waste bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 634d52224fd056c9273264277824afc2 and manufactured by VITAL HEALTHCARE SDN BHD. 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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634d52224fd056c9273264277824afc2
Registration Details
Taiwan FDA Registration: 634d52224fd056c9273264277824afc2
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Device Details

"Xingchang" plasma filtration waste bag (unsterilized)
TW: โ€œๆๆ˜Œโ€่ก€ๆผฟ้Žๆฟพๅปขๆถฒ่ข‹ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

634d52224fd056c9273264277824afc2

DHA09402027702

Company Information

Malaysia

Product Details

It is limited to the scope of the first level of identification of the "Hemodialysis System and Its Accessories (H.5820)" of the Measures for the Classification and Grading of Medical Devices.

H Gastroenterology and urology

H.5820 ่ก€ๆถฒ้€ๆž็ณป็ตฑๅŠๅ…ถ้™„ไปถ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Apr 08, 2019

Apr 08, 2024