Taiwan FDA registration e70f89f8880acbe5972779d5e0ea8e90
“LeMaitre” Aortic Occlusion Catheter
TW: “樂脈”主動脈阻斷導管
Registration details
- Analysis ID
- e70f89f8880acbe5972779d5e0ea8e90
- License Form
- Ministry of Health Medical Device Import No. 034072
- Customs Code
- DHA05603407203
Company information
- Manufacturer
- LEMAITRE VASCULAR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4450 Vascular Clip
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 05, 2020
- Expiry Date
- Nov 05, 2025
About this record
Access comprehensive regulatory information for “LeMaitre” Aortic Occlusion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e70f89f8880acbe5972779d5e0ea8e90 and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is HSIN TUNG MEDICAL 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