Taiwan FDA registration b92c8d4b6c6e17a9e680839342b497f9

"Marco" cantilever system (non-sterile)

TW: "瑪珽" 懸臂系統 (未滅菌)

Taiwan·Risk Class 1·KLS Martin SE & Co. KG;; KLS Martin SE & Co.KG·Registered Sep 20, 2024 – Sep 20, 2029Active

Registration details

Analysis ID: b92c8d4b6c6e17a9e680839342b497f9
Customs Code: DHA09402360903

Company information

Manufacturer: KLS Martin SE & Co. KG;; KLS Martin SE & Co.KG
Manufacturer Country: Germany
Authorized Representative: KINDMED CORPORATION

Product details

Intended Use: It is limited to the first level of identification of the "Electric or Pneumatic Surgical Operating Tables, Surgical Chairs and Their Accessories (I.4960)" of the Measures for the Classification and Grading of Medical Devices.
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: Sep 20, 2024
Expiry Date: Sep 20, 2029

About this record

Access comprehensive regulatory information for "Marco" cantilever system (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b92c8d4b6c6e17a9e680839342b497f9 and manufactured by KLS Martin SE & Co. KG;; KLS Martin SE & Co.KG. The authorized representative in Taiwan is KINDMED CORPORATION.

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