Taiwan FDA registration 25b31b2cefb96d076b6afe3389fe1387
V.A.C. Ulta Therapy System
TW: 奧塔沖灌洗負壓治療系統
Registration details
- Analysis ID
- 25b31b2cefb96d076b6afe3389fe1387
- License Form
- Ministry of Health Medical Device Import No. 034783
- Customs Code
- DHA05603478300
Company information
- Manufacturer
- KCI USA, Inc.;;KCI Manufacturing
- Manufacturer Country
- United States;;Ireland
- Authorized Representative
- 3M TAIWAN LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4780 powered suction pump
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 11, 2021
- Expiry Date
- Oct 11, 2026
About this record
Access comprehensive regulatory information for V.A.C. Ulta Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25b31b2cefb96d076b6afe3389fe1387 and manufactured by KCI USA, Inc.;;KCI Manufacturing. The authorized representative in Taiwan is 3M TAIWAN 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 DatabasePowered by Pure Global AI89,000+ Devices