Devices

Device Recall AXIOM ARTIS MODULAR ANGIOGRAPHIC SYSTEM

Model / Serial
Model number 7412807. Serial numbers: 35302, 35678, 35909, and 35916.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including states of AR, CA, CO, FL, IA, IL, IN, KS, KY, MI, NY, TX, VA, and WY.
Product Description
AXIOM Artis System dFC using software version VB31D with 30x40 cm2 flat detectors. || ¿AXIOM Artis is a angiography system developed for single and biplane diagnostic imaging and interventional procedures.
Manufacturer
Siemens Medical Solutions USA, Inc
1 Event
- Recall of Device Recall AXIOM ARTIS MODULAR ANGIOGRAPHIC SYSTEM

Manufacturer

Siemens Medical Solutions USA, Inc

Manufacturer Address
Siemens Medical Solutions USA, Inc, 51 Valley Stream Pkwy, Malvern PA 19355-1406
Manufacturer Parent Company (2017)
Siemens Ag
Source
USFDA

5 devices with a similar name

Learn more about the data here

Device Recall AXIOM ARTIS MODULAR ANGIOGRAPHIC SYSTEM

Model / Serial
Model number 7555357. Serial numbers: 53086, 53128, 53149, 53162, 53165, and 53194.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including states of AR, CA, CO, FL, IA, IL, IN, KS, KY, MI, NY, TX, VA, and WY.
Product Description
AXIOM Artis System dBA using software version VB31D with 30x40 cm2 flat detectors. || ¿AXIOM Artis is a angiography system developed for single and biplane diagnostic imaging and interventional procedures.
Manufacturer
Siemens Medical Solutions USA, Inc

Device Recall AXIOM ARTIS MODULAR ANGIOGRAPHIC SYSTEM

Model / Serial
Model number 7555373. Serial numbers: 50176 and 51707
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including states of AR, CA, CO, FL, IA, IL, IN, KS, KY, MI, NY, TX, VA, and WY.
Product Description
AXIOM Artis System dFA using software version VB31D with 30x40 cm2 flat detectors. || ¿AXIOM Artis is a angiography system developed for single and biplane diagnostic imaging and interventional procedures.
Manufacturer
Siemens Medical Solutions USA, Inc

Device Recall AXIOM ARTIS MODULAR ANGIOGRAPHIC SYSTEM

Model / Serial
Model number 7413078. Serial numbers: 46130, 46150, and 46205.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including states of AR, CA, CO, FL, IA, IL, IN, KS, KY, MI, NY, TX, VA, and WY.
Product Description
AXIOM Artis System dTC using software version VB31D with 30x40 cm2 flat detectors. || ¿AXIOM Artis is a angiography system developed for single and biplane diagnostic imaging and interventional procedures.
Manufacturer
Siemens Medical Solutions USA, Inc

Device Recall AXIOM ARTIS MODULAR ANGIOGRAPHIC SYSTEM

Model / Serial
Model number 7008605. Serial numbers: 55090, 55322, and 55469
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including states of AR, CA, CO, FL, IA, IL, IN, KS, KY, MI, NY, TX, VA, and WY.
Product Description
AXIOM Artis System dTA using software version VB31D with 30x40 cm2 flat detectors. || ¿AXIOM Artis is a angiography system developed for single and biplane diagnostic imaging and interventional procedures.
Manufacturer
Siemens Medical Solutions USA, Inc

Device Recall AXIOM ARTIS MODULAR ANGIOGRAPHIC SYSTEM

Model / Serial
Model number 7555365. Serial numbers: 57076, 57187, and 57188.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including states of AR, CA, CO, FL, IA, IL, IN, KS, KY, MI, NY, TX, VA, and WY.
Product Description
AXIOM Artis System dMP using software version VB31D with 30x40 cm2 flat detectors. || ¿AXIOM Artis is a angiography system developed for single and biplane diagnostic imaging and interventional procedures.
Manufacturer
Siemens Medical Solutions USA, Inc

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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