VIDCO's Protocol Converter allows researchers to acquire patient data from patient monitoring networks, including GE's Unity Network. No knowledge of the source protocols is required.

System Operation/Specification

Input(s): Unity Network Rwhat packets, Numeric Packets, Wave Packets
Outputs: VIDCO Discovery Packets, Numeric Packets, Wave Packets, Message Packets
Connections: 16 Patient monitor connections maximum per MDP2040-0216PC. Each connection will serve a single client.
Clients: If there is a need to support more than a single client per connection, the user can create their own client server from the received data and redistribute to as many additional clients as is needed.
Adding Patients: Additional MDP2040-0216PCs can be added to provide additional Patient monitor connections.

 

 

VIDCO switch connection port is configured to pass 126.255.255.255 broadcasts, and data To/From the MDP2040-0216PC(s).

Specifications

Input Protocol

GE Unity Network Protocol compatible with Solar, Dash, Eagle, Tram, B850 and Telemetry monitors running RWHAT Ver. 1.4 protocol.

 

Output Protocol

VIDCO Interface Protocol V3.0

Vital Signs

Waveforms: ECG1, ECG2, ECG3, ECGV, RESP, INVP1, INVP2, INVP3, INVP4, SPO2, CO2
Numeric Values: HR or PR, Up to 8 BPs (Sys/Dias/Mean), NIBP, ST, PVC count, SpO2, EtCO2/InCO2, O2 (Exp/Ins), CO, BT, RR, Temp (T1/T2/DT), MSPEC (Gas/Exp/Ins), BIS

Connections

16 single client connections maximum.

Physical

Size:

MDP2040-0200PC

H 1.5” (38 mm)

W 7.8” (198 mm)

D 7.9” (200 mm)

Power Adapter

H 1.3” (32 mm)

W 2.3” (58 mm)

D 4.3” (110 mm)

Weight:
1.7 lbs. (0.77 kg) 0.4 lbs. (0.18 kg)

AC Input

100-240V, .38A @ 100V, .24A @ 240V

 

Electrical Safety

Conforms to IEC 60601-1 as Class 1 device for UL 60601-1

Issued: 2003-04-25 Ed.:1 Rev:2006/04/26, CSA C22.2 NO.601.1

Environmental

Temperature:

Operating

0 to 40° C

Storage

-40 to +85° C

Humidity:

5% to 95%, non-condensing

EMC

IEC 60601-1-2:2007 Class B. CISPR 11:2009 (Amended by A1:2010)

 

FDA

Device 510K listed

 

CE/Medical Device Directive

CB Scheme testing, CE marking per Medical Device Directive, Directive 2007/47/EC Class IIb Device.

 

Quality Certification

VIDCO Inc. is certified to the ISO13485 Quality Standard