Pure Global

"Kesier" movable negative pressure assisted healing treatment device - Taiwan Registration b9c2a1e3b557011cd0442ea504922664

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..

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
b9c2a1e3b557011cd0442ea504922664
Registration Details
Taiwan FDA Registration: b9c2a1e3b557011cd0442ea504922664
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kesier" movable negative pressure assisted healing treatment device
TW: โ€œๅ‡ฑ่ฅฟ็ˆพโ€ๆดปๅ‹•ๅž‹่ฒ ๅฃ“่ผ”ๅŠฉ็™’ๅˆๆฒป็™‚ๅ„€
Risk Class 2

Registration Details

b9c2a1e3b557011cd0442ea504922664

DHA05602633003

Company Information

Ireland;;United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

I.4780 ๅ‹•ๅŠ›ๅผๆŠฝๅธๅนซๆตฆ

import

Dates and Status

Jul 07, 2014

Jul 07, 2029