So, there are the following situations with @ext:MustUnderstand and the consumer does not understand the extension: Situation | Parent | Child | Rule 1.) | false | false | consumer can use parent and child element 2.) | false | true | consumer can use parent but must ignore child element 3.) | true | false | consumer must ignore the parent and child element 4.) | true | true | consumer must ignore the parent and child element (same as 3.) If this is the correct interpretation of TR1342, I'm fine...
That clarifies it for me. Thanks!
So, there are the following situations with @ext:MustUnderstand and the consumer does not understand the extension: Situation Parent Child Rule 1.) false false consumer can use parent and child element 2.) false true consumer can use parent but must ignore child element 3.) true false consumer must ignore the parent and child element 4.) true true consumer must ignore the parent and child element (same as 3.) If this is the correct interpretation of TR1342, I'm fine with it.
Thanks for the change - that makes the statement much clearer.
Not clear what the individual purposes in the list mean
This is not what I meant with "Describe response from provider.". What I meant is shall the provider just reject the connection, or shall it allow the connection, return a meaningful error code and then close the connection.
Note that the pysiological range has no direct relationship to the alert range but can be used as a guideline for it. In my opinion, the reason for the physiological range is mainly for display purposes (e.g. inital scaling of a trend diagram). Since the physiological range is dependent on the patient category, I could imagine 2 options: 1.) the physiological range will automatically change when the patient category is changed at the device 2.) each metric has a list of physiological ranges - one...
IEEE 11073-10101 not referenced
Intended Use: Participant key purposes (3)
Intended Use: Participant key purposes (2)
Intended Use: Participant key purposes (1)
Typo: MEDCIAL IT-NETWORK
6.1.5 Ranges: clarification on Pre-Sets and Settings
TR0240: Ranges for Pre-Sets and Settings
Confused Support column with Status column
TR0257: not clear what ActivationDuration indicates?
How do indicate a stopped/interrupted measurement?
TR0239 this is a potential risk when not consider patient category
DeterminationPeriod only for waves?
Settings shall set DeterminationTime?
Confusing timestamp / mode / etc. requirements
Provide a DeterminationTime for Ongoing measurements?
Accuracy class of measurements
ConceptDescription for enumerated values
Risk of erroneous messages
When LifeTimePeriod is not set should Consumer consider risk?
Why is DeterminationTime not mandatory?
DeterminationTime property not part of the list
DeterminationTime should consider internal latency
Other means to validate device connection
Definition of appropriate use
List of supported certificate attributes/options
Definition of metric usage dependent on SafetyClassification
Change Disclaimer Wording
Localization of texts
Inconsistent use of @MustUnderstand
Definition of a ContextStateValidator
Required patient identifier up to the responsible organization
UDI on MDS level
Additional 11073 nomenclature standards
MDIB sequence relative order - why is this important?
UDI is not explained in the acronyms section
Which requirements must be listed?
What to do when exceeding the # of participant requests?
Time zone should be part of the log message entry
Log message requirements
Handling ambiguous location contexts
Differentiate between use model requirements and technical requriements
More information about inferred Participant Ensemble Context
Reference System: meaning of different SDC implementation
System clocks synchronized to commen time source
"Should" requirements only listed when implemented!?
Duplicate acronym "XML" w/ identical descriptions