"I-REP" Cold Pack (Non-Sterile) - Taiwan Registration dce03358524becca4e4a52e489a09ade

Access comprehensive regulatory information for "I-REP" 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 dce03358524becca4e4a52e489a09ade and manufactured by I-REP Therapy Products, Inc.. The authorized representative in Taiwan is ORTHOHEALTH CO., LTD..

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