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ASTM F 2401 : 2016 : REDLINE

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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Standard Practice for Security Checkpoint Metal Detector Screening of Persons with Medical Devices

Available format(s)

PDF

Superseded date

25-10-2024

Language(s)

English

Published date

01-10-2016

€67.30
Excluding VAT

CONTAINED IN VOL. 15.08, 2016 Specifies the needs and concerns of persons with implanted, active, medical devices or active ambulatory medical devices, as well as passive implanted medical devices, while maintaining the integrity of the security checkpoint.

Committee
F 12
DocumentType
Redline
Pages
6
PublisherName
American Society for Testing and Materials
Status
Superseded
SupersededBy

1.1The following practice is intended to address the needs and concerns of persons with implanted, active, medical devices or active ambulatory medical devices, as well as passive implanted medical devices, while maintaining the integrity of the security checkpoint.

1.2Active and passive implanted medical devices are being used at an increasing rate as a means to prolong and improve quality of life. Although these medical devices are typically designed to operate in the electromagnetic environment experienced in daily life, there is a potential for the disruption of active medical device function when exposed to certain electromagnetic fields emitted by commonly encountered electrically powered products, including handheld and walk-through metal detectors used in security checkpoint screening. In addition, some active or passive implanted devices may trigger the unintended alarm of the metal detector.

1.3The values stated in SI units are to be regarded as the standard. The values shown in parentheses are for information only.

1.4This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

ISO/TR 21730:2007 Health informatics Use of mobile wireless communication and computing technology in healthcare facilities Recommendations for electromagnetic compatibility (management of unintentional electromagnetic interference) with medical devices
PD ISO/TR 21730:2007 Health informatics. Use of mobile wireless communication and computing technology in healthcare facilities. Recommendations for electromagnetic compatibility (management of unintentional electromagnetic interference) with medical devices

ISO 14708-7:2013 Implants for surgery Active implantable medical devices Part 7: Particular requirements for cochlear implant systems
ISO 14708-5:2010 Implants for surgery Active implantable medical devices Part 5: Circulatory support devices
ISO 14117:2012 Active implantable medical devices Electromagnetic compatibility EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
ISO 14708-2:2012 Implants for surgery Active implantable medical devices Part 2: Cardiac pacemakers
ISO 14708-1:2014 Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
ISO 14708-3:2017 Implants for surgery — Active implantable medical devices — Part 3: Implantable neurostimulators
ISO 14708-4:2008 Implants for surgery Active implantable medical devices Part 4: Implantable infusion pumps
ISO 14708-6:2010 Implants for surgery Active implantable medical devices Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators)

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