AIRIP Medical Cold Pack (Unsterilized) - Taiwan Registration af64707a621bc63389c5738ecab4ddac
Access comprehensive regulatory information for AIRIP Medical Cold Pack (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number af64707a621bc63389c5738ecab4ddac and manufactured by I-REP Therapy Products, Inc.. The authorized representative in Taiwan is TISSUKINE 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.
Device Details
Product Details
Limited to the classification and grading management of medical equipment, the first level identification range of "Medical Hot and Cold Compress Device (O.5700)".
o Physical Medical Sciences
O.5700 ้ซ็็จๅท็ฑๆท่ฃ็ฝฎ
Dates and Status
Sep 02, 2022
Oct 31, 2025

