"Fabrication" Cold pack (Non-Sterile) - Taiwan Registration 31f5da87bbc955464ba46a3440f48d72
Access comprehensive regulatory information for "Fabrication" 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 31f5da87bbc955464ba46a3440f48d72 and manufactured by FABRICATION ENTERPRISES INCORPORATED. The authorized representative in Taiwan is GOOD LINE INCORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FABRICATION ENTERPRISES INCORPORATED, 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
Registration Details
31f5da87bbc955464ba46a3440f48d72
Ministry of Health Medical Device Import Registration No. 016980
DHA08401698008
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, 2026

