Taiwan FDA registration 492a3902aaf0cdc2db471014a928c08d

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·FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD·Registered Feb 21, 2013 – Feb 21, 2018Cancelled
Registration details
Analysis ID
492a3902aaf0cdc2db471014a928c08d
Customs Code
DHA04200048603
Company information
Manufacturer Country
China
Authorized Representative
Sunray Health Limited
Product details
Intended Use
It is used for emergency biochemical and plasma biochemical examination.
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
Feb 21, 2013
Expiry Date
Feb 21, 2018
Cancellation Date
Dec 20, 2019
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 492a3902aaf0cdc2db471014a928c08d and manufactured by FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD. The authorized representative in Taiwan is Sunray Health Limited.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HEBEI XINLE SCI&TECH 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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