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“DYNATRONICS”Cold Pack (Non-Sterile) - Taiwan Registration 099fbe98c97d6d35706ff1af0f8b190e

Access comprehensive regulatory information for “DYNATRONICS”Cold Pack (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 099fbe98c97d6d35706ff1af0f8b190e and manufactured by DYNATRONICS CORPORATION. The authorized representative in Taiwan is EVER PROSPEROUS INSTRUMENT INC..

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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099fbe98c97d6d35706ff1af0f8b190e
Registration Details
Taiwan FDA Registration: 099fbe98c97d6d35706ff1af0f8b190e
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Device Details

“DYNATRONICS”Cold Pack (Non-Sterile)
TW: “達能壯”醫療用冷敷包 (未滅菌)
Risk Class 1
MD

Registration Details

099fbe98c97d6d35706ff1af0f8b190e

Ministry of Health Medical Device Import Registration No. 007317

DHA08400731702

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "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, 2024