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Emdyca

Bioimaging and radiotherapy instrumentsDiagnostic and interventional radiology instrumentsVarious instruments for radiodiagnostics and interventional procedures

Multiple contrast agent injectors

EMDN code Z11039014

10 manufacturers, 32 models including 32 on the market, 5 countries

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Manufacturers registered in Europe (EUDAMED) 10
  • On the market
  • No longer marketed
  • 93/42 Former directive, not yet certified under the MDR
  • Click a manufacturer to see its full range, a model to open its EUDAMED record.
ManufacturerCountryRegistered modelsClassContact
Bracco FDA EU representative : ACIST Europe BV (Netherlands) Switzerland
3 others
I, IIa, IIb MDR, 93/42 Website EUDAMED record Report an error
Liebel-Flarsheim FDA EU representative : Guerbet (France) United States
2 others
IIb MDR, 93/42 EUDAMED record Report an error
Nemoto Kyorindo FDA EU representative : Medicor International NV/SA (Belgium) Japan IIb 93/42 EUDAMED record Report an error
Nanyang Clear Science Technology EU representative : WISELINK MEDICAL, S.L.U. (Spain) China IIb MDR Website sales@judcare.com EUDAMED record Report an error
Acist FDA EU representative : ACIST Europe BV (Netherlands) United States IIb 93/42 Website EUDAMED record Report an error
Anke EU representative : Shanghai International Holding Corp. GmbH(Europe) (Germany) China IIb 93/42 EUDAMED record Report an error
Medtron Germany IIb MDR Website info@medtron.com EUDAMED record Report an error
Ulrich FDA Germany IIb MDR info@ulrichmedical.com EUDAMED record Report an error
Jusha FDA EU representative : Lotus NL B.V. (Netherlands) China IIb MDR Website ra@jusha.com.cn EUDAMED record Report an error
Suzhou Hengrui Hongyuan Medical FDA EU representative : PureCE B.V. (Netherlands) China IIb MDR EUDAMED record Report an error

A model registered in EUDAMED is not necessarily sold in your country. Check availability and CE marking with the manufacturer.

Other manufacturers known in the United States (FDA) 15

Manufacturers selling this type of device in the United States according to the FDA, not yet in EUDAMED for this category. Some do sell in Europe: registration of devices already on the market is mandatory until 28 November 2026, and some are registered under their parent company’s name. The category is inferred automatically from the US classification and may include related products.

ManufacturerCountryBrandsFDA clearance
Bayer Medical Care Inc. Present in Europe in other categories United States MEDRAD® Stellant FLEX CT Injection System with Certegra® Workstation MEDRAD® Stellant FLEX Syringe Kit MEDRAD XDS Extravasation Detection System MEDRAD® Stellant FLEX CT Injection System with Certegra® Workstation (Upgrade) MEDRAD® Stellant CT Injection System registered
IMAXEON PTY LTD Present in Europe in other categories Australia MEDRAD® Centargo Patient Line MEDRAD® Centargo CT Injection System MEDRAD® Centargo Patient Line (350 cm) MEDRAD® Centargo Day Set MEDRAD® Centargo Replacement Spike K252689 (2025)
BYTEC MEDIZINTECHNIK GMBH Germany – registered
Can Technomed Trading LTD. Canada – registered
Coeur, Inc. (a wholly owned subsidiary of Illinois Tool Work United States – registered
Gerresheimer Regensburg GmbH Germany – registered
Gilero, Inc United States – registered
Guerbet LLC / Liebel-Flarsheim Company LLC United States – registered
ICU MEDICAL, INC. Present in Europe in other categories United States – registered
Infumed GmbH Germany – registered
LRE MEDICAL GMBH Germany – registered
Phillips-Medisize A/S Present in Europe in other categories United States – registered
Promepla Present in Europe in other categories Monaco – registered
Sidam Srl Present in Europe in other categories Italy – registered
VINCENT MEDICAL MANUFACTURING CO., LTD. Hong Kong SAR China – registered

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