"Stryker" ultrafine catheter
- Analysis ID
- 612b9c2a13d6216c44cf248c2aeba2d1
- Customs Code
- DHA05603029707
- Manufacturer
- Stryker Neurovascular
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
- Registration Date
- Oct 25, 2017
- Expiry Date
- Oct 25, 2027
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Access comprehensive regulatory information for "Stryker" ultrafine catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 612b9c2a13d6216c44cf248c2aeba2d1 and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Stryker Neurovascular, 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.