Taiwan FDA registration 832c5e051935330629fff96b5dd956d5
“LILY” 3D Medical Face Mask (Non-Sterile)
TW: “怡安” 立體醫用口罩 (未滅菌)
Taiwan·Risk Class 1·MD·BenQ Sanfeng Medical Equipment Co., Ltd. Taichung Factory·Registered Mar 18, 2021 – Mar 18, 2026ExpiredRegistration details
- Analysis ID
- 832c5e051935330629fff96b5dd956d5
- License Form
- Ministry of Health Medical Device Manufacturing No. 008957
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Medical Clothing (I.4040)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4040 Medical clothing
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 18, 2021
- Expiry Date
- Mar 18, 2026
About this record
Access comprehensive regulatory information for “LILY” 3D Medical Face Mask (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 832c5e051935330629fff96b5dd956d5 and manufactured by BenQ Sanfeng Medical Equipment Co., Ltd. Taichung Factory. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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