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“STERIS” Verify HPI Vaporized VH202 Process Indicator - Taiwan Registration ba1991a255f835171b0e05ef38dd0ce5

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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ba1991a255f835171b0e05ef38dd0ce5
Registration Details
Taiwan FDA Registration: ba1991a255f835171b0e05ef38dd0ce5
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Device Details

“STERIS” Verify HPI Vaporized VH202 Process Indicator
TW: “思泰瑞”低溫化學滅菌指示劑
Risk Class 2
MD

Registration Details

ba1991a255f835171b0e05ef38dd0ce5

Ministry of Health Medical Device Import No. 028060

DHA05602806000

Company Information

United Kingdom

Product Details

For details, it is Chinese approved copy of the imitation order

J General hospital and personal use equipment

J2800 Sterilization Process Indicator

Imported from abroad

Dates and Status

Jan 22, 2016

Jan 22, 2026