Taiwan FDA registration cba44935d1e1e5d2fba46f78fc09d740

"Kaiwei" introduction/drainage catheter and its accessories (unsterilized)

TW: “愷威”導入/引流導管及其附件(未滅菌)

Taiwan·Risk Class 1·KAI WEI (SHENZHEN) CO. LTD.·Registered Jun 02, 2006 – Jun 02, 2026Expired

Registration details

Analysis ID: cba44935d1e1e5d2fba46f78fc09d740
Customs Code: DHA04600025707

Company information

Manufacturer: KAI WEI (SHENZHEN) CO. LTD.
Manufacturer Country: China
Authorized Representative: UNIMAX MEDICAL SYSTEMS INC.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Classification and Grading of Medical Devices "Introduction/Drainage Catheters and Their Accessories (I.4200)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4200 Incoming/Drainage Tubes and Accessories
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Jun 02, 2006
Expiry Date: Jun 02, 2026

About this record

Access comprehensive regulatory information for "Kaiwei" introduction/drainage catheter and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cba44935d1e1e5d2fba46f78fc09d740 and manufactured by KAI WEI (SHENZHEN) CO. LTD.. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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