| Primary Device ID | 00847946016715 |
| NIH Device Record Key | a8abc463-d6b3-4454-bb61-7580b4aff16e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ZOLL CABLE |
| Version Model Number | 1001-0700 |
| 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 | true |
| 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 Humidity | Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity |
| Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity |
| Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity |
| Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00847946016715 [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 | 2014-09-24 |
| 00847946016791 | 1007-000505-01 |
| 00847946016760 | 1009-0913-02 |
| 00847946016753 | 1009-0913-01 |
| 00847946016746 | 1009-0918-01 |
| 00847946016715 | 1001-0700 |
| 00847946016685 | 1001-0196-01 |
| 00847946019891 | 1001-001194-01 |