"Stryker" Aixveta intermediary catheter
- Analysis ID
- 064feefb7723863ea7f00d7227f15b28
- Customs Code
- DHA05603731301
- Manufacturer
- Stryker Neurovascular;; InNeuroCo
- Manufacturer Country
- United States
- Authorized Representative
- Stryker (Far East) Co., Ltd. Taiwan Branch
- 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;; Contract manufacturing
- Registration Date
- Jun 24, 2024
- Expiry Date
- Jun 24, 2029
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Access comprehensive regulatory information for "Stryker" Aixveta intermediary catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 064feefb7723863ea7f00d7227f15b28 and manufactured by Stryker Neurovascular;; InNeuroCo. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Stryker Neurovascular;; InNeuroCo, and 1 recent registrations in the same category. 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.