Taiwan FDA registration 3d2c653dabeebfcaedc084924df3d604

"Blanc" Enxi Alpha embedded in the dilated balloon catheter

TW: “柏朗”恩喜阿法嵌入擴張氣球導管
Taiwan flagTaiwan·Risk Class 3·GOODMAN CO., LTD. GOODMAN RESEARCH CENTER·Registered Sep 12, 2018 – Sep 12, 2028Active
Registration details
Analysis ID
3d2c653dabeebfcaedc084924df3d604
Customs Code
DHA05603152400
Company information
Manufacturer Country
Japan
Authorized Representative
B. BRAUN TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.0005.
Import Information
import
Dates and status
Registration Date
Sep 12, 2018
Expiry Date
Sep 12, 2028
About this record

Access comprehensive regulatory information for "Blanc" Enxi Alpha embedded in the dilated balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3d2c653dabeebfcaedc084924df3d604 and manufactured by GOODMAN CO., LTD. GOODMAN RESEARCH CENTER. The authorized representative in Taiwan is B. BRAUN TAIWAN 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