Pure Global

“STERIS” Verify V24I SELF-CONTAINED Biological Monitoring - Taiwan Registration c9a0afccd0714b85fae597eef970f174

Access comprehensive regulatory information for “STERIS” Verify V24I SELF-CONTAINED Biological Monitoring in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c9a0afccd0714b85fae597eef970f174 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
c9a0afccd0714b85fae597eef970f174
Registration Details
Taiwan FDA Registration: c9a0afccd0714b85fae597eef970f174
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“STERIS” Verify V24I SELF-CONTAINED Biological Monitoring
TW: “思泰瑞”低溫滅菌生物監測組
Risk Class 2
MD

Registration Details

c9a0afccd0714b85fae597eef970f174

Ministry of Health Medical Device Import No. 028332

DHA05602833204

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

Mar 17, 2016

Mar 17, 2026