Primary Device ID | 00840241600320 |
NIH Device Record Key | de4a8aa9-6ba1-4dd0-9ef0-ce9489513fa2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Battery |
Version Model Number | 80499-003 |
Catalog Number | 80499-003 |
Company DUNS | 060944361 |
Company Name | Kestra Medical Technologies, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx | |
Phone | 1.833.692.7787 |
xx@xx.xx |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 50 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840241600320 [Primary] |
MWJ | Electrocardiograph, Ambulatory (Without Analysis) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-09-26 |
Device Publish Date | 2024-09-18 |
00840241600313 - ASSURE Wearable ECG | 2024-09-26 A wearable cardiac episode recorder |
00840241600320 - Battery | 2024-09-26A rechargeable battery that powers the ASSURE Wearable ECG |
00840241600320 - Battery | 2024-09-26 A rechargeable battery that powers the ASSURE Wearable ECG |
00840241600337 - System Cable | 2024-09-26 Provides the connection between an ASSURE Garment and a Battery |
00840241600344 - ASSURE Assist Service | 2024-09-26 The Event Response System (ERS) is a software-only powered communication system that informs a remote user responder of the occu |
00840241600382 - Kestra Provided Device Patient Application | 2024-09-26 ASSURE Patient Application for the Kestra Provided Device. |
00840241600238 - ASSURE WCD System | 2023-07-04 The ASSURE Wearable Cardioverter Defibrillator System |
00840241600283 - ASSURE Patient Application | 2023-03-21 ASSURE patient app is a component of CareStation. |
00840241600306 - CareStation Server | 2023-03-20 CareStation Server acquires and displays data from the WCD for clinicians to view. |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BATTERY 90485587 not registered Live/Pending |
HIP Innovations, LLC 2021-01-25 |
BATTERY 90232872 not registered Live/Pending |
Battery Labs, LLC 2020-10-02 |
BATTERY 88293869 not registered Live/Pending |
Battery Management Company, LLC 2019-02-08 |
BATTERY 87257978 not registered Dead/Abandoned |
Battery Mineral Resources Limited 2016-12-05 |
BATTERY 86892866 5590660 Live/Registered |
BATTERY MARKETING, INC. 2016-02-01 |
BATTERY 79127341 4493030 Live/Registered |
Oy Sinebrychoff Ab 2013-01-23 |
BATTERY 78092107 2739073 Live/Registered |
WINFIELD SOLUTIONS, LLC 2001-11-07 |
BATTERY 77791403 not registered Dead/Abandoned |
Oy Sinebrychoff Ab 2009-07-28 |
BATTERY 77223813 not registered Dead/Abandoned |
Mountain Cycle, Inc. 2007-07-06 |
BATTERY 75393618 2209013 Live/Registered |
Oy Sinebrychoff Ab 1997-11-20 |
BATTERY 75333473 2233533 Dead/Cancelled |
ZOMBA RECORDING LLC 1997-07-31 |
BATTERY 75120199 2097076 Dead/Cancelled |
Aries Manufacturing, Inc. 1996-06-17 |