Taiwan FDA registration b9c2a1e3b557011cd0442ea504922664
"Kesier" movable negative pressure assisted healing treatment device
TW: “凱西爾”活動型負壓輔助癒合治療儀
Taiwan·Risk Class 2·KCI USA, Inc.;; KCI Manufacturing·Registered Jul 07, 2014 – Jul 07, 2029ActiveRegistration details
- Analysis ID
- b9c2a1e3b557011cd0442ea504922664
- Customs Code
- DHA05602633003
Company information
- Manufacturer
- KCI USA, Inc.;; KCI Manufacturing
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- 3M Healthcare Taiwan Co., Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4780 動力式抽吸幫浦
- Import Information
- import
Dates and status
- Registration Date
- Jul 07, 2014
- Expiry Date
- Jul 07, 2029
About this record
Access comprehensive regulatory information for "Kesier" movable negative pressure assisted healing treatment device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b9c2a1e3b557011cd0442ea504922664 and manufactured by KCI USA, Inc.;; KCI Manufacturing. The authorized representative in Taiwan is 3M Healthcare Taiwan Co., Ltd..
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