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"Sterr" sterilized packaging - Taiwan Registration 98aba356654d30b5c0b4852ec0d1c9a8

Access comprehensive regulatory information for "Sterr" sterilized packaging in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 98aba356654d30b5c0b4852ec0d1c9a8 and manufactured by Sterivic Medical Co., Ltd.. The authorized representative in Taiwan is SUNDENT CORPORATION.

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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98aba356654d30b5c0b4852ec0d1c9a8
Registration Details
Taiwan FDA Registration: 98aba356654d30b5c0b4852ec0d1c9a8
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Device Details

"Sterr" sterilized packaging
TW: โ€œๆ–ฏๅพท็‘žโ€ๆป…่ŒๅŒ…่ฃ
Risk Class 2

Registration Details

98aba356654d30b5c0b4852ec0d1c9a8

DHA09200136900

Company Information

Product Details

Details are as detailed as approved Chinese instructions

J General hospital and personal use equipment

J.6850 sterilization kit

Chinese goods;; input

Dates and Status

Jun 16, 2022

Jun 16, 2027