| ARCHETYPE ID | openEHR-EHR-CLUSTER.device_details.v1 |
|---|---|
| Concept | Device details |
| Description | Additional details that relate to safety and quality issues for ongoing and repeated use of any device. |
| Use | Use to record additional details required to supplement the generic CLUSTER.device or specicalisation archetypes. The focus of this archetype is on capturing the details related maintenance, servicing, cleaning, calibration and specific details about components of the device. |
| Purpose | To record additional details related to specifications, maintenance, servicing, cleaning and calibration for any device. |
| References | HL7 International, Implementation Guide for CDA Release 2.0 Personal Healthcare Monitoring Report (PHMR) (International Realm) Draft Standard for Trial Use Release 1. 2008;[cited 2010 Feb 2 ] IEEE. Guidelines for 64-bit Global Identifier (EUI-64) Registration Authority [Internet]. [date unknown];[cited 2010 Feb 2 ] Available from: http://standards.ieee.org/regauth/oui/tutorials/EUI64.html |
| Copyright | © openEHR Foundation |
| Authors | Author name: Ian McNicoll Organisation: Ocean Informatics Email: heather.leslie@oceaninformatics.com Date originally authored: 16/08/2010 |
| Other Details Language | Author name: Ian McNicoll Organisation: Ocean Informatics Email: heather.leslie@oceaninformatics.com Date originally authored: 16/08/2010 |
| Other Details (Language Independent) |
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| Keywords | calibration, maintenance, sterilization, cleaned, service, device |
| Lifecycle | AuthorDraft |
| Language used | en |
| Citeable Identifier | 1013.1.1460 |
| items | |
| Organisation identifier | Organisation identifier: Organisation identifier for device. May be a text string or an IEEE EUI-64 identifier. Choice of:
|
| Model | Model: The model of the device. |
| Serial number | Serial number: The serial number of the device. |
| Part number | Part number: The part number of the device. |
| Manufacturer model name | Manufacturer model name: HL7 CDA compatible representation of device manufacture details. May be a simple string or contain simple markup e.g. for Continua PHMR reports: "Pulse Master 2000||584216|69854|2.1|1.1|1.0|" repesenting Model, Unspecified, SerialNumber, PartNumber, HardwareRevision, SoftwareRevision, ProtocolRevision, and ProdSpecGMDN. |
| Hardware revision | Hardware revision: The hardware revision number. |
| Software name | Software name: Software name - for compatibility with CDA POCD_MT000040. |
| Software revision | Software revision: The software revision number. |
| Protocol revision | Protocol revision: The protocol revision number. |
| Sampling frequency | Sampling frequency: The sampling frequency limits of the device. Choice of:
|
| Range | Range: The range limits of the device. Choice of:
|
| Accuracy | Accuracy: The accuracy limits of the device. Choice of:
|
| Resolution | Resolution: The resolution limits of the device. Choice of:
|
| Regulatory status | Regulatory status: Whether device is regulated or otherwise. |
| Date last cleaned/sterilized | Date last cleaned/sterilized: Date the device was last cleaned or sterilized. |
| Date last calibrated | Date last calibrated: Date the device was last calibrated. |
| Date last serviced | Date last serviced: The date the device was last serviced. |
| Serviced by | Serviced by: Details of agent who performed the servicing. Include: All not explicitly excluded archetypes |
| Additional information | Additional information: Addtional device specification information. |
| Formulae | Formulae: Details about formulae or algorithms used by the device in order to generate results/output. |
| Formula name | Formula name: Data element which is calculated or derived. |
| Formula | Formula: Formula used to calculate or derive the Calculated field. |
| Other contributors | Heather Leslie, Ocean Informatics, Australia |
| Translators |