ISO 18778:2005
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
Respiratory equipment — Infant monitors — Particular requirements
Hardcopy , PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users
30-06-2022
English, French
02-03-2005
ISO 18778:2005 specifies requirements for the safety and essential performance of monitors used to detect apparent life-threatening events in sleeping or resting children under three years of age. This International Standard applies to devices used in home care applications. These monitors are generally used without continual professional supervision.
ISO 18778:2005 also applies to the accessories, e.g. probes and cables necessary to apply the monitor to the patient. It does not apply to monitors intended for use in health care facilities/institutions.
DevelopmentNote |
Supersedes ISO/DIS 18778 (03/2005)
|
DocumentType |
Standard
|
Pages |
26
|
PublisherName |
International Organization for Standardization
|
Status |
Withdrawn
|
SupersededBy |
Standards | Relationship |
ONORM EN ISO 18778 : 2009 | Identical |
DS EN ISO 18778 : 2009 | Identical |
NBN EN ISO 18778 : 2009 | Identical |
NEN EN ISO 18778 : 2009 | Identical |
NS EN ISO 18778 : 2009 | Identical |
I.S. EN ISO 18778:2009 | Identical |
PN EN ISO 18778 : 2009 | Identical |
SN EN ISO 18778:2009 | Identical |
UNI EN ISO 18778 : 2009 | Identical |
UNE-EN ISO 18778:2009 | Identical |
SS-EN ISO 18778:2009 | Identical |
BS EN ISO 18778:2009 | Identical |
EN ISO 18778:2009 | Identical |
NF EN ISO 18778 : 2009 | Identical |
DIN EN ISO 18778:2009-08 | Identical |
UNE-EN ISO 18778:2005 | Identical |
ISO 16142-1:2016 | Medical devices — Recognized essential principles of safety and performance of medical devices — Part 1: General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards |
BS ISO 16142-1:2016 | Medical devices. Recognized essential principles of safety and performance of medical devices General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards |
IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
ISO 15001:2010 | Anaesthetic and respiratory equipment Compatibility with oxygen |
IEC 60601-1-6:2010+AMD1:2013 CSV | Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
IEC 60601-2-23:2011 | Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment |
IEC 60068-2-64:2008 | Environmental testing - Part 2-64: Tests - Test Fh: Vibration, broadband random and guidance |
IEC 60601-1-2:2014 | Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
EN 71-1:2014 | Safety of toys - Part 1: Mechanical and physical properties |
IEC 60529:1989+AMD1:1999+AMD2:2013 CSV | Degrees of protection provided by enclosures (IP Code) |
IEC 60601-2-27:2011 | Medical electrical equipment - Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment |
NFPA 53M : 1990 | FIRE HAZARDS IN OXYGEN-ENRICHED ATMOSPHERES |
ISO 9919:2005 | Medical electrical equipment Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use |
ISO 7000:2014 | Graphical symbols for use on equipment Registered symbols |
ISO 4135:2001 | Anaesthetic and respiratory equipment Vocabulary |
EN 980:2008 | Symbols for use in the labelling of medical devices |
EN 60601-1-8:2007/A11:2017 | MEDICAL ELECTRICAL EQUIPMENT - PART 1-8: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: GENERAL REQUIREMENTS, TESTS AND GUIDANCE FOR ALARM SYSTEMS IN MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS (IEC 60601-1-8:2006/A1:2012) |
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.