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“STERIS” Vaprox HC Sterilant - Taiwan Registration e03f02275e098ad523e526973fdf7ac6

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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e03f02275e098ad523e526973fdf7ac6
Registration Details
Taiwan FDA Registration: e03f02275e098ad523e526973fdf7ac6
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Device Details

“STERIS” Vaprox HC Sterilant
TW: "思泰瑞" 低溫滅菌劑
Risk Class 2
MD

Registration Details

e03f02275e098ad523e526973fdf7ac6

Ministry of Health Medical Device Import No. 026805

DHA05602680501

Company Information

United States

Product Details

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

J General hospital and personal use equipment

J6885 Liquid chemical biocide/highly disinfectant

Imported from abroad

Dates and Status

Dec 04, 2014

Dec 04, 2024