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"DJO" Aircast Cryo-cuff series (Non-Sterile) - Taiwan Registration d5ea5a8d58203cf73ece6963cdf75c98

Access comprehensive regulatory information for "DJO" Aircast Cryo-cuff series (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 d5ea5a8d58203cf73ece6963cdf75c98 and manufactured by DJO DE MEXICO, S. A. DE C. V.. The authorized representative in Taiwan is Lunxin 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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d5ea5a8d58203cf73ece6963cdf75c98
Registration Details
Taiwan FDA Registration: d5ea5a8d58203cf73ece6963cdf75c98
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Device Details

"DJO" Aircast Cryo-cuff series (Non-Sterile)
TW: "ๅธๆทๆญ" ๆ„›ๅกๅธๅ†ท็™‚่ญทๅฅ—็ณปๅˆ— (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d5ea5a8d58203cf73ece6963cdf75c98

Ministry of Health Medical Device Import No. 017463

DHA09401746302

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Medical Water Recycling Hot and Cold Compress Pack (O.5720)".

o Equipment for physical medicine

O5720 Medical Water Recycling Hot and Cold Pack

Imported from abroad

Dates and Status

Jan 25, 2017

Jan 25, 2022