Taiwan FDA registration 280158c01001af002d836fafcc3327f1
Shakespeare's CPDA1 blood collection vessel
TW: 莎仕德CPDA1血液收集容器
Taiwan·Risk Class 2·SARSTEDT AG & CO. KG·Registered May 11, 2006 – May 11, 2021CancelledRegistration details
- Analysis ID
- 280158c01001af002d836fafcc3327f1
- Customs Code
- DHA00601658307
Company information
- Manufacturer
- SARSTEDT AG & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- PAN ASIA BIOMEDICAL TECHNOLOGY INC.
Product details
- Intended Use
- A medical device used to collect and process blood samples or to separate serum or plasma from blood sample components for further testing. This device contains the anticoagulant CPDA1.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1675 Blood collection equipment
- Import Information
- import
Dates and status
- Registration Date
- May 11, 2006
- Expiry Date
- May 11, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Shakespeare's CPDA1 blood collection vessel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 280158c01001af002d836fafcc3327f1 and manufactured by SARSTEDT AG & CO. KG. The authorized representative in Taiwan is PAN ASIA BIOMEDICAL TECHNOLOGY INC..
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