Taiwan FDA registration ba2db8af20ce93e10600c7602456ae07
3M Steri-Vac Sterilizer/ Aerator GS Series
TW: 3M環氧乙烷氣體滅菌/曝氣鍋GS系列
Taiwan·Risk Class 2·MD·BENCHMARK ELECTRONICS INC.;;3M Company, 3M Health Care·Registered Jan 09, 2017 – Jan 09, 2027ActiveRegistration details
- Analysis ID
- ba2db8af20ce93e10600c7602456ae07
- License Form
- Ministry of Health Medical Device Import No. 029333
- Customs Code
- DHA05602933301
Company information
- Manufacturer Country
- United States
- Authorized Representative
- 3M TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6860 Ethylene oxide gas sterilizer
- Import Information
- Imported from abroad; Contract manufacturing
Dates and status
- Registration Date
- Jan 09, 2017
- Expiry Date
- Jan 09, 2027
About this record
Access comprehensive regulatory information for 3M Steri-Vac Sterilizer/ Aerator GS Series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba2db8af20ce93e10600c7602456ae07 and manufactured by BENCHMARK ELECTRONICS INC.;;3M Company, 3M Health Care. The authorized representative in Taiwan is 3M TAIWAN LTD..
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