AccessGUDID - DEVICE: Expression MRI Patient Monitoring System (Model 865214) (00884838016064)

GUDID

Device Identifier (DI) Information

Brand Name: Expression MRI Patient Monitoring System (Model 865214)
Version or Model: Expression MRI Patient Monitor
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 865214
Company Name: Philips Ds North America LLC

Primary DI Number: 00884838016064
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2021
Device Count: 1
Labeler D-U-N-S® Number*: 013649151 *Terms of Use

Device Description: Expression MRI Patient Vital Signs Monitor, Wireless 2.4 GHz Dual Lead ECG Capable, Wireless 2.4 GHz, Pulse Oximetry (SpO2) Capable, Integrated Non-Invasive Blood Pressure (NIBP), Advanced ECG Filter, Integrated End-Tidal CO2, Active Trend Arrows, 360 Degree Alarm light, Quick Connect Accessories, All parameters support Adult, Pediatric, Infant and Neonatal applications, 8-Hour Smart Battery Technology, One (1) year limited warranty and factory service for hardware, Patient Monitor manufactured by Philips Healthcare and branded for Invivo Corporation, anaffiliate of Philips Healthcare. The Patient Monitor is provided with Invivo's standard 1 year. Warranty,a copy of which is available upon request. Post warranty service may be purchased for the Invivo Patient Monitor at the point of sale. For service after the point-of-sale, please contact. Invivo at 1-877-468-4861 option 1, option 3.

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
33586	General-purpose multi-parameter bedside monitor	An electrically-powered device/device assembly designed for the continuous assessment of several vital physiologic parameters (e.g., ECG, blood pressure, heart rate, temperature, cardiac output, apnoea, and respiratory/anaesthetic gas concentrations) of one patient in intensive or general healthcare settings. It typically set-up by the patient bedside and often includes programmable alarms, portable radio transmitters, receivers, and antennas (telemetry systems) to allow monitoring during patient ambulation or transportation; it is not dedicated to neonatal use and is not intended to be worn on the body.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MWI	MONITOR,PHYSIOLOGICAL,PATIENT(WITHOUT ARRHYTHMIA DETECTION OR ALARMS)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 3234df41-48ec-489f-a225-ac5547692959
Public Version Date: February 01, 2024
Public Version Number: 10
DI Record Publish Date: September 30, 2016