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“STERIS” System 1 Express Sterile Processing System - Taiwan Registration 364f17d40d9d3c6e205530423a9649bc

Access comprehensive regulatory information for “STERIS” System 1 Express Sterile Processing System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 364f17d40d9d3c6e205530423a9649bc and manufactured by STERIS CANADA ULC. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STERIS CORPORATION, and 1 recent registrations in the same category. 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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364f17d40d9d3c6e205530423a9649bc
Registration Details
Taiwan FDA Registration: 364f17d40d9d3c6e205530423a9649bc
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Device Details

“STERIS” System 1 Express Sterile Processing System
TW: “思泰瑞”過醋酸滅菌鍋
Risk Class 2
MD

Registration Details

364f17d40d9d3c6e205530423a9649bc

Ministry of Health Medical Device Import No. 031907

DHA05603190700

Company Information

Canada

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 08, 2018

Dec 08, 2023

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