Taiwan FDA registration 56ccf3d3ba2f33d02be0ea7fd1aa2043
“Alvimedica” Alviguide Blue Plus Interventional Cardiology Guiding Catheter
TW: “艾微醫學”艾微改藍二代導引導管
Registration details
- Analysis ID
- 56ccf3d3ba2f33d02be0ea7fd1aa2043
- License Form
- Ministry of Health Medical Device Import No. 027607
- Customs Code
- DHA05602760702
Company information
- Manufacturer
- ALVIMEDICA TIBBI URUNLER SAN. VE DIS. TIC. A.S.
- Manufacturer Country
- Turkey
- Authorized Representative
- JENS MEDICAL CONSULTING LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1330 Catheter Lead
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 28, 2015
- Expiry Date
- Aug 28, 2020
- 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 “Alvimedica” Alviguide Blue Plus Interventional Cardiology Guiding Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 56ccf3d3ba2f33d02be0ea7fd1aa2043 and manufactured by ALVIMEDICA TIBBI URUNLER SAN. VE DIS. TIC. A.S.. The authorized representative in Taiwan is JENS MEDICAL CONSULTING LTD..
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