AAMI and Underwriters Laboratories Inc. (UL) have jointly published AAMI/UL 2800-1, Standard for Safety for Medical Device Interoperability. The first in an expected series of standards, AAMI/UL 2800-1 addresses the safety, security, and effectiveness of medical systems with interoperable elements throughout their development, deployment, assembly, and operation.
“UL is pleased to partner with AAMI on this joint standards development effort for the interoperability of medical devices,” says Phil Piqueira, vice president, UL Global Standards.
Jennifer Padberg, senior vice president, standards program and policy at AAMI, also hailed the collaborative effort. “We’re excited by this partnership with UL,” she says. “By working together, we’ve created a standard that we believe will be valuable to the medical device industry. Device interoperability remains a stubborn challenge, and we see this standard as a vital resource in achieving that goal.”
Diana Pappas Jordan, standards program manager at UL and co-chair of the 2800 Joint Committee, says that AAMI/UL 2800-1 is the result of years of development and commitment by the committee and provides a critical set of requirements for medical device interoperability.
Specifically, the standard employs a life cycle process approach to organizing requirements, providing a set of interoperability planning, realization, deployment, and monitoring activities that incorporate cross-cutting requirements for security and risk management. AAMI/UL 2800-1 also provides supplementary guidance on key clinical and engineering properties essential for ensuring effective interoperability.
Wil Vargas, standards director at AAMI and co-chair of the 2800 Joint Committee, notes that this standard was just the start of a bigger effort. “AAMI and UL have developed the foundational document that specifies a baseline set of requirements for assuring safe and secure medical device interoperability,” Vargas says. “This will serve as the cornerstone for a family of standards that will extend across different device families, as well as with different interoperability critical factors. We are excited to include this within the AAMI and UL portfolio.”
Interoperability has been discussed for decades. DICOM was created and HL-7 exists too yet full open interoperability doesn’t exist. There are too many details within all the data sets. It’s better then it was even 5 years ago and every step taken should help but it will never be plug and play. OR WILL IT?
it only exists within mfr/product lines. GE will never play nice with Philips, siemens, etc. And all of this junk chinese devices that barely work by themselves will just invite the hackers and ransomware in. Let’s create a set of standards that forces the big boys of device manufacturing to work with one another and allow an ICU to have multiple devices of multiple mfr’s that will work together to save lives and protect privacy.