Taiwan FDA registration 1de335b819ff4cc5d10aed6a7092c1f6

Ultrasonic systems for diagnostics "Siemens"

TW: “西門子”診斷用超音波系統
Taiwan flagTaiwan·Risk Class 2·SIEMENS MEDICAL SOLUTIONS USA, INC.·Registered Nov 05, 2009 – Nov 05, 2024Expired
Registration details
Analysis ID
1de335b819ff4cc5d10aed6a7092c1f6
Customs Code
DHA00602029708
Company information
Manufacturer Country
United States
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1550 Ultrasonic pulsating Duppler imaging system
Import Information
import
Dates and status
Registration Date
Nov 05, 2009
Expiry Date
Nov 05, 2024
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About this record

Access comprehensive regulatory information for Ultrasonic systems for diagnostics "Siemens" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1de335b819ff4cc5d10aed6a7092c1f6 and manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Siemens Healthineers Ltd., SIEMENS MEDICAL SOLUTIONS USA, INC.;; PLEXUS MANUFACTURING SDN. BHD., and 3 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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