Taiwan FDA registration ba1991a255f835171b0e05ef38dd0ce5
“STERIS” Verify HPI Vaporized VH202 Process Indicator
TW: “思泰瑞”低溫化學滅菌指示劑
Taiwan·Risk Class 2·MD·Albert Browne Ltd.·Registered Jan 22, 2016 – Jan 22, 2026ExpiredRegistration details
- Analysis ID
- ba1991a255f835171b0e05ef38dd0ce5
- License Form
- Ministry of Health Medical Device Import No. 028060
- Customs Code
- DHA05602806000
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
- Jan 22, 2016
- Expiry Date
- Jan 22, 2026
About this record
Access comprehensive regulatory information for “STERIS” Verify HPI Vaporized VH202 Process Indicator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba1991a255f835171b0e05ef38dd0ce5 and manufactured by Albert Browne Ltd.. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS CO., LTD..
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