Powerheart® MDLink 40-00580-01

GUDID 00812394021499

MDLink SW 12.0

Zoll Medical Corporation

External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software External defibrillator application software
Primary Device ID00812394021499
NIH Device Record Key9168b1e8-fe16-4d04-a639-b7467fc7e4db
Commercial Distribution StatusIn Commercial Distribution
Brand NamePowerheart® MDLink
Version Model Number40-00580-01
Catalog Number40-00580-01
Company DUNS055363428
Company NameZoll Medical Corporation
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 Batchfalse
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com
Phone1.262.953.3500
Emailtechsupport@cardiacscience.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100812394021499 [Primary]

FDA Product Code

MKJAutomated External Defibrillators (Non-Wearable)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-02-08
Device Publish Date2020-05-28

Devices Manufactured by Zoll Medical Corporation

00847946096168 - AED PLUS2024-04-05 AED PLUS, PS SERIES, W/AED CVR, LCD, NO VOICE RECORDING, ENGLISH, REFURB
00847946096199 - AED PLUS2024-04-05 AED PLUS, PS SERIES NO GRAPHICS, W/AED CVR, LCD, NO VOICE RCDG, ENG, REFURB
00847946096212 - AED PLUS2024-04-05 AED PLUS, PS SERIES W/BASIC CVR, LCD, VOICE RCDG, ENG, REFURB
00847946096229 - AED PLUS2024-04-05 AED PLUS, PS SERIES W/AED CVR, LCD, VOICE RCDG, ENG, REFURB
00847946096243 - AED PLUS2024-04-05 AED PLUS, PS SERIES NO GRAPHICS, W/AED CVR, LCD, VOICE RCDG, ENG
00847946096298 - AED PRO2024-04-05 AED PRO, SEMI AUTOMATIC ONLY, NO BATTERY, NO ELECTRODES, REFURB
00847946096472 - AED PRO2024-04-05 AED PRO, SEMI AUTO W/MNL OVERRIDE, NO VOICE, LCD, ENGLISH, REFURB
00847946096533 - AED PLUS2024-04-05 AED PLUS, PA SERIES, NO LCD, NO VOICE RCDG, ENG, REFURB

Trademark Results [Powerheart]

Mark Image

Registration | Serial
Company
Trademark
Application Date
POWERHEART
POWERHEART
78905168 3206323 Live/Registered
CARDIAC SCIENCE CORPORATION
2006-06-09
POWERHEART
POWERHEART
77687247 not registered Dead/Abandoned
Hunter Laboratories, Inc.
2009-03-10
POWERHEART
POWERHEART
74367566 1955504 Live/Registered
CARDIAC SCIENCE CORPORATION
1993-03-12
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