AccessGUDID - DEVICE: Remote Alert Monitor (00850016398734)

GUDID

Device Identifier (DI) Information

Brand Name: Remote Alert Monitor
Version or Model: F-RID-15-1
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: F-RID-15-1
Company Name: AMPLION CLINICAL COMMUNICATIONS, INC.

Primary DI Number: 00850016398734
Issuing Agency: GS1
Commercial Distribution End Date: December 20, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 626493555 *Terms of Use

Device Description: Firmware for Remote Input Device (RID) version 2.x, Firmware version 1.5

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
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):	No
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?
62165	Nurse call system	An assembly of electronic devices, integrated within a facility infrastructure and/or wireless network, designed to provide an audio/visual signal to summon help when activated in response to a patient’s need for (urgent) assistance. It typically consists of and/or interacts with user- or sensor-activated signal transmitters (e.g., patient-worn pendant, push-buttons, microphones, speakers, fall sensors, smoke alarm, door sensors), a network communicator, and alert communication devices (e.g., server computer, phone, dome lights, audible alarm). The device notifies medical professionals and caregivers and is intended for use in the healthcare facility.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
ILQ	System, Communication, Powered

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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: b4a6906b-0e43-4a94-bd71-d6794cce2cf2
Public Version Date: December 27, 2023
Public Version Number: 2
DI Record Publish Date: April 30, 2020