"Swick" Radiology Patient Stent (Unsterilized)
- Analysis ID
- fb02c5fb44a5d1c62e1404ee77d9d31d
- Customs Code
- DHA09402292406
- Manufacturer
- Medtec LLC, dba CIVCO Radiotherapy
- Manufacturer Country
- United States
- Authorized Representative
- SSGI TAIWAN CO.
- Intended Use
- Limited to the first level identification range of the classification and grading management measures for medical equipment "Stents for Radiology Patients (P.1830)".
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1830 放射科病患用支架
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Oct 17, 2022
- Expiry Date
- Oct 17, 2027
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Access comprehensive regulatory information for "Swick" Radiology Patient Stent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fb02c5fb44a5d1c62e1404ee77d9d31d and manufactured by Medtec LLC, dba CIVCO Radiotherapy. The authorized representative in Taiwan is SSGI TAIWAN CO..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CIVCO MEDICAL SOLUTIONS, 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.