Taiwan FDA registration 5e6adeef5095a8a8e364f38203f10e6d
“STERIS” Revital-Ox RESERT R60 Solution Test Strips
TW: “思泰瑞”高層次消毒劑測試條
Taiwan·Risk Class 2·MD·Albert Browne Ltd.·Registered Sep 08, 2019 – Sep 08, 2024ExpiredRegistration details
- Analysis ID
- 5e6adeef5095a8a8e364f38203f10e6d
- License Form
- Ministry of Health Medical Device Import No. 032838
- Customs Code
- DHA05603283802
Company information
- Manufacturer
- Albert Browne Ltd.
- Manufacturer Country
- United Kingdom
- 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)
- J2800 Sterilization Process Indicator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 08, 2019
- Expiry Date
- Sep 08, 2024
About this record
Access comprehensive regulatory information for “STERIS” Revital-Ox RESERT R60 Solution Test Strips in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e6adeef5095a8a8e364f38203f10e6d and manufactured by Albert Browne Ltd.. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS CO., LTD..
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