AccessGUDID - DEVICE: Xhibit Telemetry Receiver (10841522120190)

GUDID

Device Identifier (DI) Information

Brand Name: Xhibit Telemetry Receiver
Version or Model: Xhibit Telemetry Receiver
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 011-0247-01
Company Name: SPACELABS HEALTHCARE (WASHINGTON), INC

Primary DI Number: 10841522120190
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 145581588 *Terms of Use

Device Description: ANTENNA,UHF,450-470MHZ, ROHS, UDI

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):	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?
36365	Electrocardiography monitoring system receiver	An electrically-powered component of an electrocardiograpy telemetric monitoring system designed to wirelessly receive, consolidate, and display electrocardiographic (ECG) signals [sometimes with an additional parameter such as haemoglobin oxygen saturation (SpO2)] from a transmitter connected to a patient, typically ambulatory, for viewing at a receiving location (e.g., central station, bedside monitor).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MLD	MONITOR, ST SEGMENT WITH ALARM
MSX	SYSTEM,NETWORK AND COMMUNICATION,PHYSIOLOGICAL MONITORS
MHX	MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)
DSI	DETECTOR AND ALARM, ARRHYTHMIA

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K141156	000

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: 5efedd0b-9ce7-4351-a440-f7e58ef6859c
Public Version Date: October 25, 2023
Public Version Number: 5
DI Record Publish Date: January 23, 2017