Taiwan FDA registration f7221a575d43f891a75a2ae6c5006f6e
"Stryker" Aix reinforced long casing set
TW: “史賽克” 艾克斯加強式長型套管組
Taiwan·Risk Class 2·Stryker Neurovascular;; InNeuroCo·Registered Aug 10, 2023 – Aug 10, 2028ActiveRegistration details
- Analysis ID
- f7221a575d43f891a75a2ae6c5006f6e
- Customs Code
- DHA05603657401
Company information
- Manufacturer
- Stryker Neurovascular;; InNeuroCo
- Manufacturer Country
- United States
- Authorized Representative
- Stryker (Far East) Co., Ltd. Taiwan Branch
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
- Contract manufacturing;; input
Dates and status
- Registration Date
- Aug 10, 2023
- Expiry Date
- Aug 10, 2028
About this record
Access comprehensive regulatory information for "Stryker" Aix reinforced long casing set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f7221a575d43f891a75a2ae6c5006f6e and manufactured by Stryker Neurovascular;; InNeuroCo. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.
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