CANopen SIG contrast media injector

Scope

Enhancement and maintenance of CANopen profiles for medical add-on devices such as injector, ECG, etc.

Chairmen

vacant

Group meetings

No events found.

Minutes

Title Date Status Size Published Action
SIG contrast media injector2017-06-20Minutes116 KiB2017-07-14Login
SIG contrast media injector2017-05-05Minutes1.2 MiB2017-07-17Login
SIG contrast media injector2017-03-03Minutes4.6 MiB2017-07-17Login
SIG contrast media injector2017-02-09Minutes123 KiB2017-07-17Login
SIG contrast media injector2016-12-15Minutes118 KiB2017-07-18Login
SIG contrast media injector2016-11-03Minutes641 KiB2017-07-18Login
SIG contrast media injector2016-10-04Minutes112 KiB2017-07-18Login
SIG contrast media injector2016-07-01Minutes108 KiB2017-07-18Login
SIG contrast media injector2016-03-03Minutes4.1 MiB2017-07-18Login
SIG contrast media injector2016-02-18Minutes111 KiB2017-07-18Login
SIG contrast media injector2017-09-14Minutes566 KiB2017-09-18Login
SIG contrast media injector2017-10-06Minutes297 KiB2017-10-11Login
SIG contrast media injector2018-09-13Minutes292 KiB2018-09-17Login
SIG contrast media injector2018-10-24Minutes594 KiB2018-10-31Login
SIG contrast media injection2018-12-11Minutes439 KiB2018-12-19Login

Specifications

Title Details
Status
Size
Published
Action
CiA 425-1 version 2.1.0CANopen application profile for medical diagnostic add-on modules – Part 1: General definitions
DescriptionThe CANopen application profile for medical diagnostic add-on modules includes several parts: Part 1 describes general definitions. Part 2 defines the profile for injector devices. Devices compliant to these profiles use communication techniques, which conforms to those described in the CANopen application layer and communication profile (CiA 301). In addition, medical devices and sub-systems may use communication techniques, which conform to those described in the CANopen additional application layer functions specification (CiA 302). These specifications should be consulted in parallel to these device profile specifications.
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DS243 KiB2011-06-03Login
CiA 425-2 version 2.4.0CANopen application profile for medical diagnostic add-on modules – Part 2: Injector
DescriptionThis profile specifies the CANopen device profile for injector interface units. This profile covers injectors connected to a medical diagnostic system (angiography, computer tomography, and other medical diagnostic devices), which provide CANopen Manager functionality. If a safety-related communication is required, the injector device is compliant to the CANopen framework for safety-related communication (EN 50325-5). The definition of SRDOs (safety-related data objects) is not in the scope of this document. A prerequisite for the conformity to this CANopen device profile is conformity with the CANopen communication profile (CiA 301). Additionally, in the case that the module is programmable it shall conform to the framework for programmable CANopen devices (CiA 302). These specifications should be consulted in parallel to this device profile specification.
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DSP795 KiB2017-11-17Login
CiA 312-1 version 1.0.0CANopen profile conformance test plan – Part 1: General definitions
DescriptionThe document contains additional lower-, dynamic- and upper tests for CANopen devices that shall be tested according to a certain device profile. The definitions of the generic lower-, dynamic- and upper tests do not fall in the scope of this document.
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DSP76 KiB2008-04-11Login
CiA 312-2 version 1.0.0CANopen profile conformance test plan – Part 2: Generic I/O modules
DescriptionThis part of CANopen device profile conformance test plan contains additional tests for generic I/O modules, which are tested for conformity according to CANopen device profile generic I/O modules. The additional tests verify entries in EDS and object dictionary, which are defined in CANopen device profile generic I/O modules. Furthermore additional test steps verify object coherences that are defined in that device profile. To achieve a certain level of conformity the CANopen device shall pass the corresponding tests defined in CANopen conformance test plan plus those defined in this part of the document series.
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DSP346 KiB2008-04-11Login
CiA 312-4 version 1.0.0CANopen profile conformance test plan – Part 4: Contrast media injectors
DescriptionThis part of the test plan specifies the additional tests for contrast media injectors, which shall be tested for conformity according to CANopen application profile for medical diagnostic addon modules (CiA 425-1 version 2.0. and CiA 425-2 version 2.0.2). The additional tests verify entries in EDS and object dictionary, which are defined in CANopen application profile for medical diagnostic add-on modules. Furthermore additional test steps verify the implementation of the device finite state automata and further object coherences, which are defined in application profile for medical diagnostic add-on modules. To achieve a certain level of conformity the DUT shall pass the corresponding tests defined in CANopen conformance test plan, CiA 312-1, plus those defined in this test plan.
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DSP0.9 MiB2009-01-16Login
CiA 312-4 version 1.0.1CANopen profile conformance test plan – Part 4: Contrast media injectors
Descriptionn/a
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WD1.5 MiB2012-05-20Login
CiA 312-5 version 0.0.4CANopen device profile conformance test plan - Part 5: Special purpose car add-on device
Descriptionn/a
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WD1.8 MiB2016-06-06Login
CiA 312-6 version 0.0.1CANopen device profile conformance test plan - Part 6: SIIS level-2 devices
Descriptionn/a
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WDP719 KiB2010-05-10Login
CiA 312-7 version 0.0.3CANopen conformance test plan - Part 7: Pedelec Profile 1
Descriptionn/a
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WD468 KiB2018-08-30Login
CiA 412-1 version 1.0.0CANopen profiles for medical devices - Part 1: General definitions
DescriptionThe CANopen profiles for medical devices includes several parts: Part 1 describes general definitions. Part 2 defines the profile for automatic X-ray collimators. Part 3 defines the profile for X-ray generators. Part 4 defines the profile for patient tables. Part 5 defines the profile for X-ray stands. Devices compliant to these profiles use communication techniques, which conforms to those described in the CANopen communication profile (CiA Draft Standard DS-301, /2/). In addition, medical devices and sub-systems may use communication techniques, which conform to those described in the framework for programmable CANopen Devices (CiA Draft Standard Proposal DSP- 302). These specifications should be consulted in parallel to these device profile specifications.
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public159 KiB2005-12-31Login
CiA 412-2 version 1.0.0CANopen profiles for medical devices - Part 2: Automatic X-ray collimator
DescriptionThis document represents the CANopen device profile for generic X-ray collimators, and as such describes the generic subset of collimator functionality. A prerequisite for the conformity to this CANopen device profile is conformity with the CANopen communication profile (CiA Draft Standard DS 301). Additionally, in the case that the module is programmable it must conform to the Framework for programmable CANopen devices (CiA Draft Standard Proposal DSP 302). These specifications should be consulted in parallel to this device profile specification.
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public658 KiB2005-12-31Login
CiA 412-6 version 1.1.0CANopen profiles for medical devices - Part 6: Dose measurement system
DescriptionThis specification defines the CANopen device profile for dose measurement systems. A prerequisite for the conformity to this CANopen device profile is conformity with the CANopen communication profile. Additionally, in the case that the module is programmable conformance to the framework for programmable CANopen devices is required. It is recommended to consulted these specifications in parallel to this device profile specification.
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public0.9 MiB2008-08-27Login