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"Pewei" postoperative wound care system - Taiwan Registration 5dbc64ac0515f42d4e29382c4e1991fc

Access comprehensive regulatory information for "Pewei" 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 5dbc64ac0515f42d4e29382c4e1991fc and manufactured by KCI USA, Inc.;; KCI Manufacturing. The authorized representative in Taiwan is 3M Healthcare Taiwan Co., Ltd..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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5dbc64ac0515f42d4e29382c4e1991fc
Registration Details
Taiwan FDA Registration: 5dbc64ac0515f42d4e29382c4e1991fc
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Device Details

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

Registration Details

5dbc64ac0515f42d4e29382c4e1991fc

DHA05602881001

Company Information

Ireland;;United States

Product Details

To treat surgical incisions that still leak to the outside after sutures or staples, wound negative pressure therapy techniques are used to provide a closed environment and remove exudate.

I General, Plastic Surgery and Dermatology

I.4780 ๅ‹•ๅŠ›ๅผๆŠฝๅธๅนซๆตฆ

Input;; Contract manufacturing

Dates and Status

Jan 19, 2017

Jan 19, 2027