Taiwan FDA registration 4ca9faf5105a3b4ce1963c586e6edc8c
Yijia single-use vacuum blood collection (no additives)
TW: 醫佳一次性使用真空採血管(無添加)
Taiwan·Risk Class 2·FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD·Registered Sep 30, 2013 – Sep 30, 2018CancelledRegistration details
- Analysis ID
- 4ca9faf5105a3b4ce1963c586e6edc8c
- Customs Code
- DHA09200052101
Company information
- Manufacturer
- FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- Sunray Health Limited
Product details
- Intended Use
- Blood samples are collected and processed for further serologic testing.
- 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
- Sep 30, 2013
- Expiry Date
- Sep 30, 2018
- Cancellation Date
- Jul 15, 2022
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 (no additives) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ca9faf5105a3b4ce1963c586e6edc8c and manufactured by FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD. The authorized representative in Taiwan is Sunray Health Limited.
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