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"Pevi Home" postoperative wound care system - Taiwan Registration 4636bfaa3b89f5e01e356b6d3f1e72d4

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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4636bfaa3b89f5e01e356b6d3f1e72d4
Registration Details
Taiwan FDA Registration: 4636bfaa3b89f5e01e356b6d3f1e72d4
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Device Details

"Pevi Home" postoperative wound care system
TW: โ€œไฝฉๅจๅฎถโ€่ก“ๅพŒๅ‚ทๅฃ็…ง่ญท็ณป็ตฑ
Risk Class 2

Registration Details

4636bfaa3b89f5e01e356b6d3f1e72d4

DHA05603497506

Company Information

Ireland;;United States

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I.4780 ๅ‹•ๅŠ›ๅผๆŠฝๅธๅนซๆตฆ

Contract manufacturing;; input

Dates and Status

Oct 15, 2021

Oct 15, 2026