NF EN ISO 11073-20101 : 2006

1 Overview
   1.1 Scope
   1.2 Purpose
   1.3 Goals
   1.4 Audience
2 References
3 Definitions and abbreviations
   3.1 Definitions
   3.2 Acronyms and abbreviations
4 Conventions
5 Rationale
   5.1 Communication model
   5.2 Information model
6 Communication model
   6.1 General
   6.2 ACSE protocol
        6.2.1 General
        6.2.2 ACSE services
        6.2.3 ACSE ASN.1 message definition
        6.2.4 ACSE user information fields
   6.3 Session-layer protocol
        6.3.1 General
        6.3.2 Session-layer services
        6.3.3 Session-layer message definitions
   6.4 Presentation-layer protocol
        6.4.1 General
        6.4.2 Presentation-layer services
        6.4.3 Presentation-layer messages
   6.5 ROSE protocol
        6.5.1 General
        6.5.2 ROSE services
        6.5.3 ROSE message definitions
   6.6 CMDISE protocol (CMDIP)
        6.6.1 General
        6.6.2 CMDISE services
        6.6.3 CMDIP message definitions
        6.6.4 SNTP
7 Information model
   7.1 Object model
   7.2 Format model
        7.2.1 Syntax
        7.2.2 Compatibility
8 Conformance
   8.1 Scope
   8.2 Object identifier administration
   8.3 MDAP subset conformance
   8.4 Implementation conformance
Annex A (normative) Medical device encoding
                      rules (MDER)
Annex B (normative) Allocation of identifiers
Annex C (informative) Time synchronization
Annex D (informative) Dynamic model
Annex E (normative) Abstract syntax
Annex F (informative) PDU examples
Annex G (informative) Specialization of ASN.1
Annex H (informative) Compatibility cases
Annex I (informative) Bibliography