Taiwan FDA registration 2b3b3602fafe071fed9234bd07020122
"STERIS" Revital-Ox Resert High Level Disinfectant
TW: “思泰瑞”高層次消毒劑
Taiwan·Risk Class 2·MD·STERIS CORPORATION·Registered May 11, 2017 – May 11, 2027ActiveRegistration details
- Analysis ID
- 2b3b3602fafe071fed9234bd07020122
- License Form
- Ministry of Health Medical Device Import No. 029718
- Customs Code
- DHA05602971805
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
- May 11, 2017
- Expiry Date
- May 11, 2027
About this record
Access comprehensive regulatory information for "STERIS" Revital-Ox Resert High Level Disinfectant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b3b3602fafe071fed9234bd07020122 and manufactured by STERIS CORPORATION. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS CO., LTD..
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