Taiwan FDA registration df88c4454d8fe70478e8a93d600bac4c

"Cellulent" epidermal sleeve set (sterilized)

TW: "賽祿通" 表皮取皮套組 (滅菌)

Taiwan·Risk Class 1·KCI USA, Inc.;; KCI Manufacturing·Registered Jul 05, 2016 – Jul 05, 2026Expired

Registration details

Analysis ID: df88c4454d8fe70478e8a93d600bac4c
Customs Code: DHA09401674102

Company information

Manufacturer: KCI USA, Inc.;; KCI Manufacturing
Manufacturer Country: Ireland;;United States
Authorized Representative: 3M Healthcare Taiwan Co., Ltd.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4820 Surgical Appliances and Accessories or Accessories
Import Information: 委託製造;; 輸入;; QMS/QSD

Dates and status

Registration Date: Jul 05, 2016
Expiry Date: Jul 05, 2026

About this record

Access comprehensive regulatory information for "Cellulent" epidermal sleeve set (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number df88c4454d8fe70478e8a93d600bac4c and manufactured by KCI USA, Inc.;; KCI Manufacturing. The authorized representative in Taiwan is 3M Healthcare Taiwan Co., Ltd..

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