Taiwan FDA registration 4636bfaa3b89f5e01e356b6d3f1e72d4
"Pevi Home" postoperative wound care system
TW: “佩威家”術後傷口照護系統
Taiwan·Risk Class 2·KCI USA, Inc.;; KCI Manufacturing·Registered Oct 15, 2021 – Oct 15, 2026ActiveRegistration details
- Analysis ID
- 4636bfaa3b89f5e01e356b6d3f1e72d4
- Customs Code
- DHA05603497506
Company information
- Manufacturer
- KCI USA, Inc.;; KCI Manufacturing
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- 3M Healthcare Taiwan Co., Ltd.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Contract manufacturing;; input
Dates and status
- Registration Date
- Oct 15, 2021
- Expiry Date
- Oct 15, 2026
About this record
Access comprehensive regulatory information for "Pevi Home" postoperative wound care system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4636bfaa3b89f5e01e356b6d3f1e72d4 and manufactured by KCI USA, Inc.;; KCI Manufacturing. The authorized representative in Taiwan is 3M Healthcare Taiwan Co., Ltd..
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