Taiwan FDA registration ae2207fd7d7c4a336929413ecd3bc75b

“Siemens” Diagnostic Ultrasound Catheter

TW: “西門子”超音波導管
Taiwan flagTaiwan·Risk Class 2·MD·Siemens Healthineers Ltd.·Registered Dec 02, 2013 – Dec 02, 2023Expired
Registration details
Analysis ID
ae2207fd7d7c4a336929413ecd3bc75b
License Form
Ministry of Health Medical Device Import No. 025649
Customs Code
DHA05602564905
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E1200 Diagnostic endovascular catheter
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 02, 2013
Expiry Date
Dec 02, 2023
Companies making similar products

Top companies providing products similar to "“Siemens” Diagnostic Ultrasound Catheter"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for “Siemens” Diagnostic Ultrasound Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae2207fd7d7c4a336929413ecd3bc75b and manufactured by Siemens Healthineers Ltd.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Siemens Healthineers Ltd., 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations