Taiwan FDA registration f587daa0f04bd851ce0e7686bdccdaad

"Steril" cantilever system (unsterilized)

TW: "思泰瑞" 懸臂系統 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·STERIS SAS·Registered Jan 25, 2022 – Jan 25, 2027Active
Registration details
Analysis ID
f587daa0f04bd851ce0e7686bdccdaad
Customs Code
DHA09402273809
Company information
Manufacturer
STERIS SAS
Manufacturer Country
France
Authorized Representative
MEDTRUST INTERNATIONAL CO., LTD.
Product details
Intended Use
Limited to the classification and grading management of medical equipment, the first level identification range of "electric or pneumatic surgical tables, surgical chairs and their accessories (I.4960)".
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4960 Electric or pneumatic surgical tables, surgical chairs, and accessories thereof
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Jan 25, 2022
Expiry Date
Jan 25, 2027
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About this record

Access comprehensive regulatory information for "Steril" cantilever system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f587daa0f04bd851ce0e7686bdccdaad and manufactured by STERIS SAS. The authorized representative in Taiwan is MEDTRUST INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STERIS SURGICAL TECHNOLOGIES SAS, 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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