Taiwan FDA registration e8994220df4e31013efe29a091c59533

"Aquan" introduction/drainage catheter and its accessories (sterilization)

TW: "亞康恩" 導入/引流導管及其附件 (滅菌)

Taiwan·Risk Class 1·ARGON MEDICAL DEVICES, INC.·Registered Aug 01, 2014 – Aug 01, 2029Active

Registration details

Analysis ID: e8994220df4e31013efe29a091c59533
Customs Code: DHA09401439700

Company information

Manufacturer: ARGON MEDICAL DEVICES, INC.
Manufacturer Country: United States
Authorized Representative: CHINA SPRING TRADING CO., LTD.

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: QMS/QSD;; 輸入

Dates and status

Registration Date: Aug 01, 2014
Expiry Date: Aug 01, 2029

About this record

Access comprehensive regulatory information for "Aquan" introduction/drainage catheter and its accessories (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e8994220df4e31013efe29a091c59533 and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..

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