Taiwan FDA registration 721ccc4562ee09281c2c5581640c836b
"Fibli Kaixun" Medical Hot & Moist Pack (Unsterilized)
TW: "菲布利凱迅" 醫療用濕熱敷包 (未滅菌)
Registration details
- Analysis ID
- 721ccc4562ee09281c2c5581640c836b
- Customs Code
- DHA08401884308
Company information
- Manufacturer
- FABRICATION ENTERPRISES INC.
- Manufacturer Country
- United States
- Authorized Representative
- GOOD LINE INCORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the "Medical Hot and Humid Compress Pack (O.5730)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5730 醫療用濕熱敷包
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Fibli Kaixun" Medical Hot & Moist Pack (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 721ccc4562ee09281c2c5581640c836b 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