Monitoring Waveform Viewer

GUDID 00812345029819

Cardiology Data Management System

MORTARA INSTRUMENT, INC.

Patient monitoring system module, electrocardiographic, telemetric Patient monitoring system module, electrocardiographic, telemetric
Primary Device ID00812345029819
NIH Device Record Key69007fd3-90e7-4206-9cbf-bade668ece0e
Commercial Distribution StatusIn Commercial Distribution
Brand NameMonitoring Waveform Viewer
Version Model Number11093-002-50
Company DUNS062046149
Company NameMORTARA INSTRUMENT, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone888-667-8272
Emailtechsupport@mortara.com
Phone888-667-8272
Emailtechsupport@mortara.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100812345029819 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MHXMonitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-06-29
Device Publish Date2016-09-24

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