Pure Global

"Sterix" biosterilization indicator group - Taiwan Registration 01812c6ce4b7a2c44d8a5412fae144cd

Access comprehensive regulatory information for "Sterix" biosterilization indicator group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 01812c6ce4b7a2c44d8a5412fae144cd 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
01812c6ce4b7a2c44d8a5412fae144cd
Registration Details
Taiwan FDA Registration: 01812c6ce4b7a2c44d8a5412fae144cd
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Sterix" biosterilization indicator group
TW: โ€œๆ€ๆณฐ็‘žโ€็”Ÿ็‰ฉๆป…่ŒๆŒ‡็คบๅŠ‘็ต„
Risk Class 2

Registration Details

01812c6ce4b7a2c44d8a5412fae144cd

DHA00602394302

Company Information

United States

Product Details

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

J General hospital and personal use equipment

J.2800 Sterilization Process Indicator

import

Dates and Status

Aug 28, 2012

Aug 28, 2027