Injector, Contrast Medium, Automatic

Spike for CT (CM/NaCl) for ulrichINJECT CT injectors

Registry build 21.09.26
1manufacturer
5catalogue numbers in this listing
7510(k) clearances naming this product code

Who Else Makes It

Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code IZQ
Manufacturer City Province Registered as Device types
Vincent Medical (Dong Guan) Manufacturing Co., Ltd. Dong Guan Guangdong Contract manufacturer 29

Record

Regulatory record for Injector, Contrast Medium, Automatic
Listed by Ulrich Gmbh & Co. KG, Germany
FDA product code IZQ
Device type Injector, Contrast Medium, Automatic
Device class Class 2
Regulation 21 CFR 870.1650
Establishment Contract manufacturer, Manufacturer, Exporter
510(k) K171392
Record published 2019-03-12
Record revised 2025-12-16 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Packaging Pack of 100, pack of 10, pack of 80, pack of 30, pack of 240

Catalogue Numbers

Catalogue numbers for Injector, Contrast Medium, Automatic
Catalogue number Size Status
XD 2037 In distribution
XD 8002 In distribution
XD 2047 In distribution
XD 8132 In distribution
XD 2042 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
LF Liebel-Flarsheim Company LLC 16
ulrich medical disposables Ulrich Gmbh & Co. KG 9
ulricheasyINJECT Max Ulrich Gmbh & Co. KG 3
Remote Control Bracco Injeneering 3
Floor Stand Bracco Injeneering 3
FastLoad™ MR Syringe Pack Bracco Injeneering 3
EmpowerCTA®+ Injector System Bracco Injeneering 3
Medrad® Stellant Flex Syringe Kit Bayer Medical Care Inc. 3
Hydraulic Controller Bracco Injeneering 2
Day Set III HP Bracco Injeneering 2
EmpowerMR® Injector System without Remote Control Bracco Injeneering 2
Medrad XDS Extravasation Detection System Bayer Medical Care Inc. 2

Showing 12 of 38. All products under Injector, Contrast Medium, Automatic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252281 2025-11-18
K251295 2025-11-07
K241850 2024-08-26
K233737 2024-04-19
K210541 2021-08-06
K192872 2020-07-02
K171392 2017-11-09

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer