Taiwan FDA registration 53af6e4df39682a773e6a10ec86b967a
“Lily” Feed tube guide (Non-Sterile)
TW: “怡安”餵食引導器 (未滅菌)
Taiwan·Risk Class 2·MD·LILY MEDICAL CORPORATION·Registered May 10, 2023 – May 10, 2028ActiveRegistration details
- Analysis ID
- 53af6e4df39682a773e6a10ec86b967a
- License Form
- Ministry of Health Medical Device Manufacturing No. 007861
Company information
- Manufacturer
- LILY MEDICAL CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LILY MEDICAL CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H5980 Gastrointestinal tubes and their accessories
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 10, 2023
- Expiry Date
- May 10, 2028
About this record
Access comprehensive regulatory information for “Lily” Feed tube guide (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 53af6e4df39682a773e6a10ec86b967a and manufactured by LILY MEDICAL CORPORATION. The authorized representative in Taiwan is LILY MEDICAL 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