Taiwan FDA registration 2de158d7a44f8799e2f766d291a3c134
Yijia single-use vacuum blood collection (sodium citrate 1:4)
TW: 醫佳一次性使用真空採血管(檸檬酸鈉1:4)
Taiwan·Risk Class 2·FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD·Registered Nov 30, 2011 – Nov 30, 2021CancelledRegistration details
- Analysis ID
- 2de158d7a44f8799e2f766d291a3c134
- Customs Code
- DHA04200041302
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
- Chinese goods;; input
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 (sodium citrate 1:4) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2de158d7a44f8799e2f766d291a3c134 and manufactured by FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD. The authorized representative in Taiwan is Sunray Health Limited.
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