"Po Ling" Medical Cold Pack (Unsterilized) - Taiwan Registration ff068b963db7143fac9e6c2784e041e3
Access comprehensive regulatory information for "Po Ling" 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 ff068b963db7143fac9e6c2784e041e3 and manufactured by FUSO TEIYAKU QINGDAO CO., LTD.. The authorized representative in Taiwan is PANION & BF BIOTECH INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUSO TEIYAKU QINGDAO CO., LTD., and 1 recent registrations in the same category. 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 first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".
o Physical Medical Sciences
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Dates and Status
Dec 04, 2018
Dec 04, 2023
Sep 30, 2021
Cancellation Information
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