Taiwan FDA registration b20e82d2877ccf4c001e81114333ec57
"CelluTome" Epidermal Harvesting System (Sterile)
TW: "賽祿通" 表皮取皮套組 (滅菌)
Taiwan·Risk Class 1·MD·KCI USA, Inc.;;KCI Manufacturing·Registered Jul 05, 2016 – Jul 05, 2026ExpiredRegistration details
- Analysis ID
- b20e82d2877ccf4c001e81114333ec57
- License Form
- Ministry of Health Medical Device Import No. 016741
- Customs Code
- DHA09401674102
Company information
- Manufacturer
- KCI USA, Inc.;;KCI Manufacturing
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- 3M TAIWAN LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4820 Surgical Appliance Motors with Accessories or Accessories
- Import Information
- Imported from abroad; Contract manufacturing;; GMP
Dates and status
- Registration Date
- Jul 05, 2016
- Expiry Date
- Jul 05, 2026
About this record
Access comprehensive regulatory information for "CelluTome" Epidermal Harvesting System (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b20e82d2877ccf4c001e81114333ec57 and manufactured by KCI USA, Inc.;;KCI Manufacturing. The authorized representative in Taiwan is 3M TAIWAN LTD..
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