Taiwan FDA registration fb02c5fb44a5d1c62e1404ee77d9d31d

"Swick" Radiology Patient Stent (Unsterilized)

TW: "思威克" 放射科病患用支架 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Medtec LLC, dba CIVCO Radiotherapy·Registered Oct 17, 2022 – Oct 17, 2027Active
Registration details
Analysis ID
fb02c5fb44a5d1c62e1404ee77d9d31d
Customs Code
DHA09402292406
Company information
Manufacturer Country
United States
Authorized Representative
SSGI TAIWAN CO.
Product details
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
Dates and status
Registration Date
Oct 17, 2022
Expiry Date
Oct 17, 2027
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About this record

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.

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