MDDS – Medical Device Data Connectivity (MDDS classification*)
We interface with laboratory machines, intravenous pumps, image acquisition machines, machines that read and measure patient vital signs. More generally, we connect today to well over 90% of the medical machines used for intensive care in Europe and America.
What is OSSI offering?
OneSource Solutions International(OSSI) offers direct connectivity with medical devices (multi-parameter monitors, anesthesia machines, BIS, ventilators, thermometers, blood pressure gauges) from various manufacturers such as GE, Siemens, Draeger, DatexOhmeda, Nihon Kohden, Mindray.
OSSI is able to interface with laboratory machines, intravenous pumps, image acquisition machines, machines that read and measure patient vital signs. More generally, OSSI is able to connect today to well over 90% of the medical machines used for intensive care in Europe and America. OSSI offers the connectivity solution commonly classified as medical middleware, placing itself technologically between the medical record, or more generally the information systems, and the various medical machines and clinical resources existing today, and is open to future ones. Medical devices of different manufacturers and of different technological status often have proprietary protocols and inadequate protection towards the network. Generally, the data collected need some transformation and integration before being used by the medical records.
Medical Connectivity
Patient Monitor
GE, Philips, Mindray, Drager, Spacelabs, Nihon Kohden, …
Anesthesia
Drager, Mindray, GE, DatexOhmeda, …
Ventilators
BP, Drager, GE, Philips, DatexOhmeda, Maquet, GEM, …
BIS and other vial sign monitors
Aspect, Nellcore, Medrad, Ikaria, …
Labs
ABL, Onyx, Cobas, Massimo, JBA, Stat, …
ECMO
Maquet …
Our connectivity hardware follows the FDA’s Medical Device Quality System and Design Control Guidance For Medical Device Manufacturer regulations, and will take actions to classify the OneSource IOT under the MDDS Rule.
Risks mitigated with MDDS include the potential for inaccurate, incomplete, or untimely data transfer, storage, conversion, or display of medical device data – making sure that our project “does not distort the values of the values obtained from the equipment.