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Single-use vacuum blood collection (separating gel/coagulant) - Taiwan Registration d48689da4ca21acb897498b5689ccb5a

Access comprehensive regulatory information for Single-use vacuum blood collection (separating gel/coagulant) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d48689da4ca21acb897498b5689ccb5a and manufactured by HEBEI XINLE SCI & TECH CO., LTD.. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD, HEBEI XINLE SCI&TECH CO., LTD., and 2 recent registrations in the same category. 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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d48689da4ca21acb897498b5689ccb5a
Registration Details
Taiwan FDA Registration: d48689da4ca21acb897498b5689ccb5a
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Device Details

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

Registration Details

d48689da4ca21acb897498b5689ccb5a

DHA09200099109

Company Information

Product Details

This product is used to take and collect blood for serum biochemical testing.

A Clinical chemistry and clinical toxicology

A.1675 Blood collection equipment

Input;; Chinese goods

Dates and Status

Nov 30, 2018

Nov 30, 2028

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