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“Cramer”Flex-I Cold Packs (Non-Sterile) - Taiwan Registration cf09795e7969289d619c2d7c03956727

Access comprehensive regulatory information for “Cramer”Flex-I Cold Packs (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cf09795e7969289d619c2d7c03956727 and manufactured by CRAMER PROUCTS, INC.. The authorized representative in Taiwan is ACCURATUS INTERNATIONAL HEALTH COMPANY.

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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cf09795e7969289d619c2d7c03956727
Registration Details
Taiwan FDA Registration: cf09795e7969289d619c2d7c03956727
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Device Details

“Cramer”Flex-I Cold Packs (Non-Sterile)
TW: “克拉瑪”冰敷袋 (未滅菌)
Risk Class 1
MD

Registration Details

cf09795e7969289d619c2d7c03956727

Ministry of Health Medical Device Import Registration No. 004630

DHA08400463004

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Medical Cold Compress Pack (O.5700)".

o Equipment for physical medicine

O5700 Medical Cold Pack

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026