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“STERIS” Bowie Dick Test Pack - Taiwan Registration 830bf35d23fbfb9bfe6fe9a5d9f7a953

Access comprehensive regulatory information for “STERIS” Bowie Dick Test Pack in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 830bf35d23fbfb9bfe6fe9a5d9f7a953 and manufactured by STERIS BIOLOGICAL OPERATIONS. 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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830bf35d23fbfb9bfe6fe9a5d9f7a953
Registration Details
Taiwan FDA Registration: 830bf35d23fbfb9bfe6fe9a5d9f7a953
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Device Details

“STERIS” Bowie Dick Test Pack
TW: “思泰瑞”抽真空測試包
Risk Class 2
MD

Registration Details

830bf35d23fbfb9bfe6fe9a5d9f7a953

Ministry of Health Medical Device Import No. 030146

DHA05603014602

Company Information

United States

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

Aug 30, 2017

Aug 30, 2022