Taiwan FDA registration e0b1dda12b87e44821f3a31243397d1f
CADD-Legacy Duodopa Pump and accessories
TW: 多度寧輸液幫浦及其附件
Taiwan·Risk Class 2·MD·SMITHS MEDICAL ASD, INC.·Registered May 09, 2016 – May 09, 2021CancelledRegistration details
- Analysis ID
- e0b1dda12b87e44821f3a31243397d1f
- License Form
- Ministry of Health Medical Device Import No. 028566
- Customs Code
- DHA05602856603
Company information
- Manufacturer
- SMITHS MEDICAL ASD, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ABBVIE BIOPHARMACEUTICALS GMBH TAIWAN BRANCH (SWITZERLAND)
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5725 Infusion pump
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 09, 2016
- Expiry Date
- May 09, 2021
- Cancellation Date
- Jun 21, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for CADD-Legacy Duodopa Pump and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e0b1dda12b87e44821f3a31243397d1f and manufactured by SMITHS MEDICAL ASD, INC.. The authorized representative in Taiwan is ABBVIE BIOPHARMACEUTICALS GMBH TAIWAN BRANCH (SWITZERLAND).
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