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Single-use vacuum blood collection (coagulant) - Taiwan Registration dc816e25d75c980f581d0061385559e8

Access comprehensive regulatory information for Single-use vacuum blood collection (coagulant) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc816e25d75c980f581d0061385559e8 and manufactured by HEBEI XINLE SCI & TECH CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, 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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dc816e25d75c980f581d0061385559e8
Registration Details
Taiwan FDA Registration: dc816e25d75c980f581d0061385559e8
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Device Details

Single-use vacuum blood collection (coagulant)
TW: ้†ซๅ‡กไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(ไฟƒๅ‡ๅŠ‘)
Risk Class 2

Registration Details

dc816e25d75c980f581d0061385559e8

DHA09200061405

Company Information

Product Details

It is used for serum biochemistry (liver function, kidney function, heart function, metabolism, etc.), electrolytes, thyroid function, AIDS monitoring, tumor markers, serum immunological examination of blood collection tubes.

A Clinical chemistry and clinical toxicology

A.1675 Blood collection equipment

Chinese goods;; input

Dates and Status

May 29, 2014

May 29, 2029