Taiwan FDA registration 752741d0f2b4b8d3f9905c144cd9cf43

Yijia single-use vacuum blood collection (heparin sodium)

TW: 醫佳一次性使用真空採血管(肝素鈉)
Taiwan flagTaiwan·Risk Class 2·HEBEI XINLE SCI&TECH CO., LTD.·Registered Aug 05, 2014 – Aug 05, 2019Cancelled
Registration details
Analysis ID
752741d0f2b4b8d3f9905c144cd9cf43
Customs Code
DHA09200061902
Company information
Manufacturer Country
China
Authorized Representative
AGREE HEALTH CARE TECHNOLOGY, LTD.
Product details
Intended Use
It is used for emergency biochemical and plasma biochemical examination of blood collection tubes.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1675 Blood collection equipment
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Aug 05, 2014
Expiry Date
Aug 05, 2019
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for Yijia single-use vacuum blood collection (heparin sodium) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 752741d0f2b4b8d3f9905c144cd9cf43 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, 1 companies making similar products including FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD, and 1 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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