Taiwan FDA registration 16990393cbed2b0cfdb464acdef606eb
Ota flush negative pressure treatment system
TW: 奧塔沖灌洗負壓治療系統
Registration details
- Analysis ID
- 16990393cbed2b0cfdb464acdef606eb
- Customs Code
- DHA05603478300
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
- import
Dates and status
- Registration Date
- Oct 11, 2021
- Expiry Date
- Oct 11, 2026
About this record
Access comprehensive regulatory information for Ota flush negative pressure treatment system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16990393cbed2b0cfdb464acdef606eb 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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