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"Fabrication" Cold pack (Non-Sterile) - Taiwan Registration 8ffebdc0e3e08c49d747d6f941e1131b

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 8ffebdc0e3e08c49d747d6f941e1131b 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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8ffebdc0e3e08c49d747d6f941e1131b
Registration Details
Taiwan FDA Registration: 8ffebdc0e3e08c49d747d6f941e1131b
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Device Details

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

Registration Details

8ffebdc0e3e08c49d747d6f941e1131b

Ministry of Health Medical Device Import No. 016980

DHA09401698004

Company Information

United States

Product Details

o Equipment for physical medicine

O5700 Medical Cold Pack

Imported from abroad

Dates and Status

Sep 08, 2016

Sep 08, 2026

Cancellation Information

Logged out

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