"Fabrication" Cold pack (Non-Sterile)
Taiwan·Risk Class 1·MD·FABRICATION ENTERPRISES INCORPORATED·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- 31f5da87bbc955464ba46a3440f48d72
- License Form
- Ministry of Health Medical Device Import Registration No. 016980
- Customs Code
- DHA08401698008
- Manufacturer
- FABRICATION ENTERPRISES INCORPORATED
- Manufacturer Country
- United States
- Authorized Representative
- GOOD LINE INCORPORATION
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5700 Medical Cold Pack
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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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.