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"STERIS" Revital-Ox Resert High Level Disinfectant - Taiwan Registration 2b3b3602fafe071fed9234bd07020122

Access comprehensive regulatory information for "STERIS" Revital-Ox Resert High Level Disinfectant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b3b3602fafe071fed9234bd07020122 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.

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2b3b3602fafe071fed9234bd07020122
Registration Details
Taiwan FDA Registration: 2b3b3602fafe071fed9234bd07020122
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Device Details

"STERIS" Revital-Ox Resert High Level Disinfectant
TW: โ€œๆ€ๆณฐ็‘žโ€้ซ˜ๅฑคๆฌกๆถˆๆฏ’ๅŠ‘
Risk Class 2
MD

Registration Details

2b3b3602fafe071fed9234bd07020122

Ministry of Health Medical Device Import No. 029718

DHA05602971805

Company Information

United States

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

May 11, 2017

May 11, 2027