Taiwan FDA registration b5e2e63d853088a23a32fa09243f9ee6

“ClearStream” Bard LTX 035 Drug Coated Balloon PTA Catheter

TW: “清流” 巴德路透尼斯035經皮穿刺血管成形術藥物塗層球囊導管
Taiwan flagTaiwan·Risk Class 2·MD·CLEARSTREAM TECHNOLOGIES LTD.·Registered Mar 17, 2015 – Mar 17, 2020Cancelled
Registration details
Analysis ID
b5e2e63d853088a23a32fa09243f9ee6
License Form
Ministry of Health Medical Device Import No. 027225
Customs Code
DHA05602722501
Company information
Manufacturer Country
Ireland
Authorized Representative
BARD PACIFIC HEALTH CARE CO., LTD.
Product details
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E1250 Percutaneous catheter
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 17, 2015
Expiry Date
Mar 17, 2020
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
許可證逾有效期未申請展延
About this record

Access comprehensive regulatory information for “ClearStream” Bard LTX 035 Drug Coated Balloon PTA Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5e2e63d853088a23a32fa09243f9ee6 and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE 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