Logo
Login Sign Up
Current Revision

AAMI ANSI/AAMI 2700-2-1:2022

Medical devices and medical systems—Essential safety and performance requirements for equipment comprising the patient-centric integrated clinical environment (ICE): Part 2-1: Particular requirements for forensic data logging
Best Price Guarantee
Instant

$267.00

2-5 Days

$267.00

SAVE 10%

$480.60


Sub Total (1 Item(s))

$ 0.00

Estimated Shipping

$ 0.00

Total (Pre-Tax)

$ 0.00


or
Assoc. for the Advancement of Medical Instrumentation Logo

AAMI ANSI/AAMI 2700-2-1:2022

Medical devices and medical systems—Essential safety and performance requirements for equipment comprising the patient-centric integrated clinical environment (ICE): Part 2-1: Particular requirements for forensic data logging

PUBLISH DATE 2022
AAMI ANSI/AAMI 2700-2-1:2022
ANSI/2700-2-1 is part of the 2700 family of standards to achieve safe integrated clinical environments (ICE) (ANSI/2700-1). It was developed by the Interoperability Working Group (IOWG, SM-WG03) and is intended for use by medical device and platform manufacturers and system integrators. It provides requirements for the recording, storage, and playback of data to support safety, quality assurance, and forensic analysis for medical devices, applications, and platforms. This document supports safe and secure device interoperability by providing general functional, performance, security, and interoperability requirements of ICE data logging systems. It requires that logged data to be time-synchronized. Data may include patient waveform and parameters, images and video, configuration, settings, device capabilities of each ICE-connected device, and user and patient interactions with each device (e.g., button presses).
SDO AAMI: Assoc. for the Advancement of Medical Instrumentation
Document Number 292227
Publication Date April 22, 2022
Language en - English
Page Count
Revision Level
Supercedes
Committee
Publish Date Document Id Type View
April 22, 2022 Revision