Taiwan FDA registration 1ebc5e4a804f296393122e07c68acf18
"Edward" Modi-Mei Central Intravenous Catheter Group
TW: "愛德華"莫迪-美中央靜脈輸注導管組
Taiwan·Risk Class 2·EDWARDS LIFESCIENCES TECHNOLOGY SARL·Registered Jan 27, 2004 – Jan 27, 2019CancelledRegistration details
- Analysis ID
- 1ebc5e4a804f296393122e07c68acf18
- Customs Code
- DHA00601052107
Company information
- Manufacturer
- EDWARDS LIFESCIENCES TECHNOLOGY SARL
- Manufacturer Country
- United States
- Authorized Representative
- EDWARDS LIFESCIENCES (TAIWAN) CORPORATION
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- import
Dates and status
- Registration Date
- Jan 27, 2004
- Expiry Date
- Jan 27, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Edward" Modi-Mei Central Intravenous Catheter Group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1ebc5e4a804f296393122e07c68acf18 and manufactured by EDWARDS LIFESCIENCES TECHNOLOGY SARL. The authorized representative in Taiwan is EDWARDS LIFESCIENCES (TAIWAN) 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