Home GUDID 00847946021504 ECG
Primary DI 00847946021504
Brand ECG
Company Zoll Medical Corporation
Model 9500-000693
Device description CABLE, 3 LEAD ECG/ESU, R SERIES
Published 2016-09-16
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true Product Codes# Code, Name table Code Name DQA Oximeter DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive) DRT MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM) LDD Dc-Defibrillator, Low-Energy, (Including Paddles) LIX Aid, Cardiopulmonary Resuscitation MKJ Automated External Defibrillators (Non-Wearable)
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DQA Oximeter Cardiovascular 2 DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive) Cardiovascular 2 DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) Cardiovascular 2 LDD Dc-Defibrillator, Low-Energy, (Including Paddles) Cardiovascular 2 LIX Aid, Cardiopulmonary Resuscitation Cardiovascular 2 MKJ Automated External Defibrillators (Non-Wearable) Cardiovascular 3
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00847946021504 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00847946021504 00847946021504 847946021504 0847946021504
GMDN Terms# Term, Definition table Term Definition Rechargeable professional automated external defibrillator A portable electronic device designed to automatically detect cardiac arrhythmias (ventricular fibrillation/pulseless ventricular tachycardia) in a sudden cardiac arrest (SCA) patient, after which it audibly/visually instructs an operator to enable it to activate defibrillation of the heart through application of electrical shocks to the chest surface. The device is intended to be operated by healthcare professionals (e.g., paramedics, medical staff) in healthcare settings. It consists of an external pulse generator (EPG) and a pair of skin-adhesive electrodes to monitor the rhythm and deliver the shocks; it also includes internal rechargeable batteries that must be charged when not in use.
Storage And Handling# Type, Low, High table Type Low High Condition Handling Environment Temperature 0 Degrees Celsius 0 Degrees Celsius Storage Environment Atmospheric Pressure 0 KiloPascal 0 Storage Environment Humidity 0 Percent (%) Relative Humidity 0 Percent (%) Relative Humidity Storage Environment Temperature 0 Degrees Celsius 0 Degrees Celsius
Regulatory Flags# DUNS number 055363428 Device count 1 Lot or batch true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 20884838115389 Nasal Alar SpO2 Sensor Philips Medizin Systeme Böblingen GmbH DQA 2026-10-16 20884838115396 Nasal Alar SpO2 Sensor Philips Medizin Systeme Böblingen GmbH DQA 2026-10-16 06946725572818 APK APK Technology Co.,Ltd. DQA 2026-10-14 06946725572825 APK APK Technology Co.,Ltd. DQA 2026-10-14 06946725572801 APK APK Technology Co.,Ltd. DQA 2026-10-09 07290019919346 OxSat100 S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD DQA 2026-10-07 07290019919414 OxSat100 S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD DQA 2026-10-07 07290019919421 OxSat100 S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD DQA 2026-10-07 07290019919438 OxSat100 S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD DQA 2026-10-07 00195278949752 TruSignal SpO2 MM 3.0M GE Healthcare Finland Oy DRT 2026-10-04 00195278949752 TruSignal SpO2 MM 3.0M GE Healthcare Finland Oy DQA 2026-10-04 00195278949769 TruSignal SpO2 MM 1.8M GE Healthcare Finland Oy DQA 2026-10-04 00195278949769 TruSignal SpO2 MM 1.8M GE Healthcare Finland Oy DRT 2026-10-04 00198953002186 Carescape Dock F0 GE Healthcare Finland Oy DQA 2026-10-04 00198953002186 Carescape Dock F0 GE Healthcare Finland Oy DRT 2026-10-04 00198953009567 Carescape ONE GE Healthcare Finland Oy DRT 2026-10-04 00198953009567 Carescape ONE GE Healthcare Finland Oy DQA 2026-10-04 00847946050740 ZENIX Zoll Medical Corporation MKJ 2026-09-25 06946725547168 APK APK Technology Co.,Ltd. DQA 2026-09-24 06946725571705 APK APK Technology Co.,Ltd. DQA 2026-09-20 06946725571903 APK APK Technology Co.,Ltd. DQA 2026-09-20 07290016714265 SleepSense S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD DQA 2026-09-08 06946725538005 APK APK Technology Co.,Ltd. DQA 2026-09-04 06946725548998 APK APK Technology Co.,Ltd. DQA 2026-09-04 06946725572276 APK APK Technology Co.,Ltd. DQA 2026-09-04 00847946030926 ZENIX Zoll Medical Corporation MKJ 2026-08-26 00884838126275 PHILIPS HeartStart SMARTPADS II PHILIPS ELECTRONICS NORTH AMERICA CORPORATION MKJ 2026-08-26 00884838126282 PHILIPS HeartStart SMARTPADS III PHILIPS ELECTRONICS NORTH AMERICA CORPORATION MKJ 2026-08-26 00884838126299 FR2/FR2+ Adult Electrode Pads PHILIPS ELECTRONICS NORTH AMERICA CORPORATION MKJ 2026-08-26 00884838126473 PHILIPS HeartStart SMARTPADS III PHILIPS ELECTRONICS NORTH AMERICA CORPORATION MKJ 2026-08-26