Taiwan FDA registration a73260cc346937a99ba4ae7348aa78c9

"Intec" submarine peripheral vascular therapy catheter

TW: “英泰克”潛艇週邊血管治療導管
Taiwan flagTaiwan·Risk Class 2·INVATEC S.p.A.·Registered Dec 18, 2008 – Dec 18, 2013Cancelled
Registration details
Analysis ID
a73260cc346937a99ba4ae7348aa78c9
Customs Code
DHA00601950808
Company information
Manufacturer
INVATEC S.p.A.
Manufacturer Country
Italy
Authorized Representative
MEDTRONIC (TAIWAN) 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.1250 Percutaneous catheters
Import Information
import
Dates and status
Registration Date
Dec 18, 2008
Expiry Date
Dec 18, 2013
Cancellation Date
Nov 15, 2016
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Intec" submarine peripheral vascular therapy catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a73260cc346937a99ba4ae7348aa78c9 and manufactured by INVATEC S.p.A.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Invatec S.p.A., and 1 recent registrations in the same category. 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.

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