Taiwan FDA registration bbe7107937949fe1499221c33681dcb3
"Fabrication" Moist Heat Pack (Non-Sterile)
TW: "菲布利凱迅" 醫療用濕熱敷包 (未滅菌)
Taiwan·Risk Class 1·MD·FABRICATION ENTERPRISES INC.·Registered Feb 27, 2018 – Feb 27, 2023CancelledRegistration details
- Analysis ID
- bbe7107937949fe1499221c33681dcb3
- License Form
- Ministry of Health Medical Device Import No. 018843
- Customs Code
- DHA09401884304
Company information
- Manufacturer
- FABRICATION ENTERPRISES INC.
- Manufacturer Country
- United States
- Authorized Representative
- GOOD LINE INCORPORATION
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5730 Thermal and moist compress for medical use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 27, 2018
- Expiry Date
- Feb 27, 2023
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Fabrication" Moist Heat 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 bbe7107937949fe1499221c33681dcb3 and manufactured by FABRICATION ENTERPRISES INC.. The authorized representative in Taiwan is GOOD LINE INCORPORATION.
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices