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"Sterry" ethylene oxide (ethylene oxide) sterilizer/aerator - Taiwan Registration fc8fb99a6d6dcdf9fe9cf2357c6d699f

Access comprehensive regulatory information for "Sterry" ethylene oxide (ethylene oxide) sterilizer/aerator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc8fb99a6d6dcdf9fe9cf2357c6d699f 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.

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fc8fb99a6d6dcdf9fe9cf2357c6d699f
Registration Details
Taiwan FDA Registration: fc8fb99a6d6dcdf9fe9cf2357c6d699f
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Device Details

"Sterry" ethylene oxide (ethylene oxide) sterilizer/aerator
TW: โ€œๆ€ๆณฐ็‘žโ€ ็’ฐๆฐงไน™็ƒท(ๆฐงๅŒ–ไน™็ƒฏ)ๆป…่Œ้‹/ๆ›ๆฐฃๆฉŸ
Risk Class 2
Cancelled

Registration Details

fc8fb99a6d6dcdf9fe9cf2357c6d699f

DHA00602460602

Company Information

Product Details

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

J General hospital and personal use equipment

J.6860 ็’ฐๆฐงไน™็ƒทๆฐฃ้ซ”ๆป…่Œๅ™จ

import

Dates and Status

Jul 11, 2013

Jul 11, 2018

Jun 16, 2022

Cancellation Information

Logged out

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