Devices

IGUIDE 2.2.0

Model / Serial
Model: , Affected: using iGUIDE 2.2.0, iGUIDE 2.2.1
Manufacturer
Elekta Inc
1 Event
- Recall of IGUIDE 2.2.0

Manufacturer

Elekta Inc

Manufacturer Parent Company (2017)
Elekta AB
Source
NZMMDSA

2 devices with a similar name

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iGuide 2.1.0 and iGuide 2.2.0

Model / Serial
Product Description
iGuide 2.1.0 and iGuide 2.2.0, Medical Intelligence Medizintechnik GmbH
Manufacturer
Elekta Pte Ltd

iGUIDE software 2.2(sites using iGUIDE 2.2.0 and 2.2.1)

Model / Serial
iGUIDE software 2.2(sites using iGUIDE 2.2.0 and 2.2.1)Reference Number: FCA-MI-0003ARTG Number 187340
Product Classification
Radiology Devices
Manufacturer
Elekta Pty Ltd

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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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