Taiwan FDA registration 17f25c2b68d32545500174961a281067
Yijia single-use vacuum blood collection blood collection (dipotassium ethylenediaminetetraacetate)
TW: 醫佳一次性使用真空採血管(乙二胺四乙酸二鉀)
Taiwan·Risk Class 2·FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD·Registered Feb 21, 2013 – Feb 21, 2018CancelledRegistration details
- Analysis ID
- 17f25c2b68d32545500174961a281067
- Customs Code
- DHA04200048705
Company information
- Manufacturer
- FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- Sunray Health Limited
Product details
- Intended Use
- It is used for the examination of blood routine [red blood cells, white blood cells, platelets, white blood cell differential, hemoglobin].
- 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
About this record
Access comprehensive regulatory information for Yijia single-use vacuum blood collection blood collection (dipotassium ethylenediaminetetraacetate) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17f25c2b68d32545500174961a281067 and manufactured by FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD. The authorized representative in Taiwan is Sunray Health Limited.
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