| Primary Device ID | 00847946016708 |
| NIH Device Record Key | ea42503c-a914-44e5-b4bb-9f07f1cd58d8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ZOLL BATTERY LI-ION |
| Version Model Number | 1017-001100-01 |
| Company DUNS | 055363428 |
| Company Name | Zoll Medical Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Storage Environment Atmospheric Pressure | Between 0 KiloPascal and 0 |
| Storage Environment Atmospheric Pressure | Between 0 KiloPascal and 0 |
| Storage Environment Atmospheric Pressure | Between 0 KiloPascal and 0 |
| Storage Environment Atmospheric Pressure | Between 0 KiloPascal and 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00847946016708 [Primary] |
| MKJ | Automated external defibrillators (non-wearable) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2014-09-23 |
| 00847946099480 | 1017-001100-01 |
| 00847946016838 | 1008-002003-30 |
| 00847946016821 | 1008-002003-01 |
| 00847946016784 | 1009-001535-03 |
| 00847946016708 | 1017-001100-01 |
| 00847946049881 | BATTERY, LITHIUM ION, SUREPOWER II RECONDITIONED |
| 00847946049898 | BATTERY, LI-ION 9 CELL 18650, RECONDITIONED |