Taiwan FDA registration cd609e2113dfc9e60f3b7aab90f89221
“Stryker” AXS Infinity LS Long Sheath
TW: “史賽克” 艾克斯長型套管組
Taiwan·Risk Class 2·MD·Stryker Neurovascular·Registered Sep 24, 2021 – Sep 24, 2026ActiveRegistration details
- Analysis ID
- cd609e2113dfc9e60f3b7aab90f89221
- License Form
- Ministry of Health Medical Device Import No. 034865
- Customs Code
- DHA05603486502
Company information
- Manufacturer
- Stryker Neurovascular
- Manufacturer Country
- Ireland
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 24, 2021
- Expiry Date
- Sep 24, 2026
About this record
Access comprehensive regulatory information for “Stryker” AXS Infinity LS Long Sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cd609e2113dfc9e60f3b7aab90f89221 and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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