| 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 |
| 00840241600399 - Kestra Provided Device Patient Application | 2025-05-08 ASSURE Patient Application for the Kestra Provided Device. |
| 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. |
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 |