Taiwan FDA registration 207543a6d4403888e0d2f047c04622be
“LILY” Needleless Connector
TW: “怡安”無針輸液連接頭
Taiwan·Risk Class 2·MD·LILY MEDICAL CORPORATION·Registered Jul 14, 2016 – Jul 14, 2026ExpiredRegistration details
- Analysis ID
- 207543a6d4403888e0d2f047c04622be
- License Form
- Ministry of Health Medical Device Manufacturing No. 005380
Company information
- Manufacturer
- LILY MEDICAL CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LILY MEDICAL CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5440 Intravascular infusion sleeve
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 14, 2016
- Expiry Date
- Jul 14, 2026
About this record
Access comprehensive regulatory information for “LILY” Needleless Connector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 207543a6d4403888e0d2f047c04622be 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