Pure Global

“STERIS” V-PRO 60 Low Temperature Sterilization System - Taiwan Registration 29776b3b79fef60f54d25bc9ffec3a32

Access comprehensive regulatory information for “STERIS” V-PRO 60 Low Temperature Sterilization System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 29776b3b79fef60f54d25bc9ffec3a32 and manufactured by STERIS MEXICO, S. DE R. L. DE C.V.. 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
29776b3b79fef60f54d25bc9ffec3a32
Registration Details
Taiwan FDA Registration: 29776b3b79fef60f54d25bc9ffec3a32
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“STERIS” V-PRO 60 Low Temperature Sterilization System
TW: “思泰瑞”汽化過氧化氫低溫滅菌鍋
Risk Class 2
MD

Registration Details

29776b3b79fef60f54d25bc9ffec3a32

Ministry of Health Medical Device Import No. 028552

DHA05602855205

Company Information

Product Details

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

J General hospital and personal use equipment

J6860 Ethylene oxide gas sterilizer

Imported from abroad

Dates and Status

Apr 28, 2016

Apr 28, 2026