Taiwan FDA registration 18c33a8d7ceecc691ee7114d3681e765
"Fengwei" Scar Gel (Non-sterilized)
TW: "灃濰" 疤痕凝膠(未滅菌)
Registration details
- Analysis ID
- 18c33a8d7ceecc691ee7114d3681e765
Company information
- Manufacturer
- COSMO BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Fengwei Medical Equipment Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Scar Treatment Silicone Products (I.4025)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4025 Silicone products for scar treatment
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Oct 04, 2023
- Expiry Date
- Oct 04, 2028
About this record
Access comprehensive regulatory information for "Fengwei" Scar Gel (Non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18c33a8d7ceecc691ee7114d3681e765 and manufactured by COSMO BIOTECH CO., LTD.. The authorized representative in Taiwan is Fengwei Medical Equipment Co., Ltd.
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