Taiwan FDA registration 8ffebdc0e3e08c49d747d6f941e1131b

"Fabrication" Cold pack (Non-Sterile)

TW: "菲布利凱迅" 醫療用冷敷包(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·FABRICATION ENTERPRISES INCORPORATED·Registered Sep 08, 2016 – Sep 08, 2026Cancelled
Registration details
Analysis ID
8ffebdc0e3e08c49d747d6f941e1131b
License Form
Ministry of Health Medical Device Import No. 016980
Customs Code
DHA09401698004
Company information
Manufacturer Country
United States
Authorized Representative
GOOD LINE INCORPORATION
Product details
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O5700 Medical Cold Pack
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 08, 2016
Expiry Date
Sep 08, 2026
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

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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