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"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.

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31f5da87bbc955464ba46a3440f48d72
Registration Details
Taiwan FDA Registration: 31f5da87bbc955464ba46a3440f48d72
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Device Details

"Fabrication" Cold pack (Non-Sterile)
TW: "่ฒๅธƒๅˆฉๅ‡ฑ่ฟ…" ้†ซ็™‚็”จๅ†ทๆ•ทๅŒ…(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

31f5da87bbc955464ba46a3440f48d72

Ministry of Health Medical Device Import Registration No. 016980

DHA08401698008

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, 2026

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