Taiwan FDA registration b628978882506b3e57d7052f491332d4
The second generation of "Epter" is an extension of the guide
TW: “埃普特” 二代導引延伸導管
Taiwan·Risk Class 2·APT Medical Inc.·Registered Mar 01, 2024 – Mar 01, 2029ActiveRegistration details
- Analysis ID
- b628978882506b3e57d7052f491332d4
- Customs Code
- DHA09200152205
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
- Chinese goods;; input
Dates and status
- Registration Date
- Mar 01, 2024
- Expiry Date
- Mar 01, 2029
About this record
Access comprehensive regulatory information for The second generation of "Epter" is an extension of the guide in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b628978882506b3e57d7052f491332d4 and manufactured by APT Medical Inc.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY CO., LTD..
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