Taiwan FDA registration ab50985bf07e8f82965fcbc495ac7ccc
"Smith" implantation infusion system
TW: “史密斯”內植用輸液系統
Registration details
- Analysis ID
- ab50985bf07e8f82965fcbc495ac7ccc
- Customs Code
- DHA00601774703
Company information
- Manufacturer
- SMITHS MEDICAL ASD, INC.
- Manufacturer Country
- United States
- Authorized Representative
- JASON'S MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5965 Subcutaneous implantable intravascular injection port and guide
- Import Information
- import
Dates and status
- Registration Date
- Jan 31, 2007
- Expiry Date
- Jan 31, 2012
- Cancellation Date
- Apr 03, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Smith" implantation infusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab50985bf07e8f82965fcbc495ac7ccc and manufactured by SMITHS MEDICAL ASD, INC.. The authorized representative in Taiwan is JASON'S MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices