Taiwan FDA registration d8df103d09c0392f7e3f4f2148149bcf

"Medtronic" suction catheter

TW: “美敦力”吸除導管
Taiwan flagTaiwan·Risk Class 2·MEDTRONIC VASCULAR·Registered Aug 24, 2007 – Aug 24, 2017Cancelled
Registration details
Analysis ID
d8df103d09c0392f7e3f4f2148149bcf
Customs Code
DHA00601821909
Company information
Manufacturer
MEDTRONIC VASCULAR
Manufacturer Country
United States
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.5150 血栓切除術導管
Import Information
import
Dates and status
Registration Date
Aug 24, 2007
Expiry Date
Aug 24, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Medtronic" suction catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d8df103d09c0392f7e3f4f2148149bcf and manufactured by MEDTRONIC VASCULAR. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC VASCULAR, 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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