Taiwan FDA registration e36dcd43c1a45131d4ac3e65d6d09ee2

Yijia disposable human venous blood sample collection container (heparin lithium / isolate gel)

TW: 醫佳一次性使用人體靜脈血樣採集容器(肝素鋰/分離膠)
Taiwan flagTaiwan·Risk Class 2·FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD·Registered Aug 14, 2012 – Aug 14, 2017Cancelled
Registration details
Analysis ID
e36dcd43c1a45131d4ac3e65d6d09ee2
Customs Code
DHA04200041802
Company information
Manufacturer Country
China
Authorized Representative
Sunray Health Limited
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
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 14, 2012
Expiry Date
Aug 14, 2017
Cancellation Date
Dec 20, 2019
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for Yijia disposable human venous blood sample collection container (heparin lithium / isolate gel) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e36dcd43c1a45131d4ac3e65d6d09ee2 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. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices