AccessGUDID - DEVICE: SmartLinx Vitals Plus (03615040000278)

GUDID

Device Identifier (DI) Information

Brand Name: SmartLinx Vitals Plus
Version or Model: SL-VP-BPAP-HW
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: Philips North America LLC

Primary DI Number: 03615040000278
Issuing Agency: GS1
Commercial Distribution End Date: January 21, 2026
Device Count: 1
Labeler D-U-N-S® Number*: 001291111 *Terms of Use
Previous DI: 03615040000230

Device Description: VitalsPlus NiBP Suntech Thermometer Exergen with RollStand

Device Characteristics

What MRI safety information does the labeling contain?	MR Unsafe
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?
36862	Patient monitoring system module, interfacing	A small unit dedicated to making communication possible between the patient monitoring system and other independent devices (e.g., ventilator, infusion pump, gas analyser, display monitors) connected to the same patient, creating an interface. It is designed to operate as part of a patient monitoring system enhancing the function of this system (the parent device) by providing connection between disparate devices. It may also be known as a medical information bus protocol.	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: 56f856b5-fe01-44d7-85f8-34eb7bb7b688
Public Version Date: January 22, 2026
Public Version Number: 5
DI Record Publish Date: April 27, 2017