Taiwan FDA registration e03f02275e098ad523e526973fdf7ac6
“STERIS” Vaprox HC Sterilant
TW: "思泰瑞" 低溫滅菌劑
Taiwan·Risk Class 2·MD·STERIS Corporation·Registered Dec 04, 2014 – Dec 04, 2024ExpiredRegistration details
- Analysis ID
- e03f02275e098ad523e526973fdf7ac6
- License Form
- Ministry of Health Medical Device Import No. 026805
- Customs Code
- DHA05602680501
Company information
- Manufacturer
- STERIS Corporation
- Manufacturer Country
- United States
- Authorized Representative
- CHUNG TENG MEDICAL INSTRUMENTS CO., 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)
- J6885 Liquid chemical biocide/highly disinfectant
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 04, 2014
- Expiry Date
- Dec 04, 2024
About this record
Access comprehensive regulatory information for “STERIS” Vaprox HC Sterilant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e03f02275e098ad523e526973fdf7ac6 and manufactured by STERIS Corporation. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS CO., LTD..
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