Taiwan FDA registration c1526b29c486e35cf9d1ea1d0badd3d2
"Epter" Tresford peripheral vascular expansion balloon catheter
TW: “埃普特” 特雷斯福特周邊血管擴張球囊導管
Taiwan·Risk Class 2·APT Medical Inc.·Registered Aug 30, 2024 – Aug 30, 2029ActiveRegistration details
- Analysis ID
- c1526b29c486e35cf9d1ea1d0badd3d2
- Customs Code
- DHA09200159404
Company information
- Manufacturer
- APT Medical Inc.
- Manufacturer Country
- China
- Authorized Representative
- NO.1 BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 30, 2024
- Expiry Date
- Aug 30, 2029
About this record
Access comprehensive regulatory information for "Epter" Tresford peripheral vascular expansion balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c1526b29c486e35cf9d1ea1d0badd3d2 and manufactured by APT Medical Inc.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY CO., LTD..
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