Taiwan FDA registration dfc50272928a61fea19ee235d1ba9014
Yijia single-use vacuum blood collection tube (tripotassium ethylenediaminetetraacetate)
TW: 醫佳一次性使用真空採血管(乙二胺四乙酸三鉀)
Taiwan·Risk Class 2·FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD·Registered Nov 30, 2011 – Nov 30, 2021CancelledRegistration details
- Analysis ID
- dfc50272928a61fea19ee235d1ba9014
- Customs Code
- DHA04200041404
Company information
- Manufacturer
- FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD
- 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
- Nov 30, 2011
- Expiry Date
- Nov 30, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Yijia single-use vacuum blood collection tube (tripotassium ethylenediaminetetraacetate) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dfc50272928a61fea19ee235d1ba9014 and manufactured by FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD. The authorized representative in Taiwan is Sunray Health Limited.
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