Taiwan FDA registration 6759e29fade5b0a893d75a2661c4e11d
"Strauss" laser separation sheath group
TW: “史特勞斯”雷射分離鞘組
Taiwan·Risk Class 2·SPECTRANETICS CORPORATION·Registered Nov 15, 2010 – Nov 15, 2025ExpiredRegistration details
- Analysis ID
- 6759e29fade5b0a893d75a2661c4e11d
- Customs Code
- DHA00602178602
Company information
- Manufacturer
- SPECTRANETICS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- LORION ENTERPRISES INC.
Product details
- Intended Use
- The Spectranetics laser separation sheath set is used with a traditional lead removal tool for patients who are suitable for intravenous removal of long-term implanted rhythmic/implantable paced defibrillator leads, including their silicone or polyurethane insulated coats.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Nov 15, 2010
- Expiry Date
- Nov 15, 2025
About this record
Access comprehensive regulatory information for "Strauss" laser separation sheath group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6759e29fade5b0a893d75a2661c4e11d and manufactured by SPECTRANETICS CORPORATION. The authorized representative in Taiwan is LORION ENTERPRISES INC..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices