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"Cellulent" epidermal sleeve set (sterilized) - Taiwan Registration df88c4454d8fe70478e8a93d600bac4c

Access comprehensive regulatory information for "Cellulent" epidermal sleeve set (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number df88c4454d8fe70478e8a93d600bac4c 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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df88c4454d8fe70478e8a93d600bac4c
Registration Details
Taiwan FDA Registration: df88c4454d8fe70478e8a93d600bac4c
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Device Details

"Cellulent" epidermal sleeve set (sterilized)
TW: "่ณฝ็ฅฟ้€š" ่กจ็šฎๅ–็šฎๅฅ—็ต„ (ๆป…่Œ)
Risk Class 1

Registration Details

df88c4454d8fe70478e8a93d600bac4c

DHA09401674102

Company Information

Ireland;;United States

Product Details

Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".

I General, Plastic Surgery and Dermatology

I.4820 Surgical Appliances and Accessories or Accessories

ๅง”่จ—่ฃฝ้€ ;; ่ผธๅ…ฅ;; QMS/QSD

Dates and Status

Jul 05, 2016

Jul 05, 2026