AAMI ISO 5840 :2005
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES
Hardcopy , PDF
03-30-2016
English
01-01-2010
Glossary of equivalent standards
Committee representation
Background on AAMI adoption of ISO 5840:2005
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Abbreviations
5 Fundamental requirements
6 Device description
6.1 Intended use
6.2 Design inputs
6.2.1 Operational specifications
6.2.2 Performance specifications
6.2.3 Packaging, labeling, and sterilization
6.3 Design outputs
6.3.1 General
6.3.2 Examples of components of some heart
valve substitutes
6.4 Design transfer (manufacturing qualification)
6.5 Risk management
6.5.1 Hazard identification
6.5.2 Failure mode identification
6.5.3 Risk estimation
6.5.4 Risk evaluation
6.5.5 Risk control
6.5.6 Risk review
7 Verification testing and analysis/Design validation
7.1 General requirements
7.2 In vitro assessment
7.2.1 Test conditions, sample selection, and
reporting requirements
7.2.2 Material property assessment
7.2.3 Hydrodynamic performance assessment
7.2.4 Structural performance assessment
7.3 Preclinical in vivo evaluation
7.3.1 Overall requirements
7.3.2 Methods
7.3.3 Test report
7.4 Clinical investigation
7.4.1 Principle
7.4.2 General
7.4.3 Number of institutions
7.4.4 Number of patients
7.4.5 Duration of the study
7.4.6 Clinical data requirements
7.4.7 Clinical investigation report
Annexes
A Rationale for the provisions of this International
Standard
B Heart valve substitute hazards, associated failure
modes, and evaluation methods
C Risk assessment guidelines
D Examples and definitions of some physical and material
properties of heart valve substitutes and their components
E Statistical procedures when using performance criteria
F In vitro procedures for testing unstented or similar
valves in compliant chambers
G Preclinical in vivo tests
H Echocardiographic protocol
I Description of the heart valve substitute
J Figures of examples of components of some heart valve
substitutes
K Examples of standards applicable to testing of materials
and components of some heart valve substitutes
L Guidelines for verification of hydrodynamic performance
M Durability testing
N Examples of design specific testing
O Fatigue assessment
P Packaging
Q Labeling and instructions for use
R Methods of evaluating clinical data
S Sterilization
Bibliography
Pertains to all devices intended for implantation in human hearts, as a heart valve substitute.
Committee |
WG 01
|
DevelopmentNote |
Supersedes AAMI CVP3 (07/2002)
|
DocumentType |
Standard
|
Pages |
85
|
ProductNote |
Reconfirmed 2005
|
PublisherName |
Association for the Advancement of Medical Instrumentation
|
Status |
Superseded
|
SupersededBy | |
Supersedes |
Standards | Relationship |
ISO 5840:2005 | Identical |
EN 12442-3 : 2000 | ANIMAL TISSUES AND THEIR DERIVATIVES UTILIZED IN THE MANUFACTURE OF MEDICAL DEVICES - PART 3: VALIDATION OF THE ELIMINATION AND/OR INACTIVATION OF VIRUSES AND TRANSMISSIBLE AGENTS |
ISO 14160:2011 | Sterilization of health care products Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives Requirements for characterization, development, validation and routine control of a sterilization process for medical devices |
ISO 11135:2014 | Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices |
ISO 13485:2016 | Medical devices Quality management systems Requirements for regulatory purposes |
ISO 14937:2009 | Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects Part 1: General requirements |
ISO 10993-2:2006 | Biological evaluation of medical devices — Part 2: Animal welfare requirements |
ISO 14630:2012 | Non-active surgical implants — General requirements |
ISO/IEC Guide 51:2014 | Safety aspects — Guidelines for their inclusion in standards |
ISO 8601:2004 | Data elements and interchange formats Information interchange Representation of dates and times |
ISO 532:1975 | Acoustics Method for calculating loudness level |
ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
ISO 11607:2003 | Packaging for terminally sterilized medical devices |
EN 12442-1 : 2000 | ANIMAL TISSUES AND THEIR DERIVATIVES UTILIZED IN THE MANUFACTURE OF MEDICAL DEVICES - PART 1: ANALYSIS AND MANAGEMENT OF RISK |
ISO 11134:1994 | Sterilization of health care products — Requirements for validation and routine control — Industrial moist heat sterilization |
ISO 14971:2007 | Medical devices Application of risk management to medical devices |
MIL-STD-1629 Revision A:1980 | PROCEDURES FOR PERFORMING A FAILURE MODE, EFFECTS AND CRITICALITY ANALYSIS |
ISO 11137:1995 | Sterilization of health care products Requirements for validation and routine control Radiation sterilization |
IEC 60651:1979+AMD1:1993+AMD2:2000 CSV | Sound level meters |
EN 12442-2 : 2000 | ANIMAL TISSUES AND THEIR DERIVATIVES UTILIZED IN THE MANUFACTURE OF MEDICAL DEVICES - PART 2: CONTROLS ON SOURCING, COLLECTION AND HANDLING |
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