| Primary Device ID | 30815098021568 |
| NIH Device Record Key | d2f00eb4-b4de-40d4-8cd6-c42bf3386d0a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pads, DDU-29XX series, universal pad, 10 pairs |
| Version Model Number | DDP-2004 |
| Company DUNS | 128340200 |
| Company Name | DEFIBTECH, L.L.C. |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 30815098021568 [Primary] |
| MKJ | Automated External Defibrillators (Non-Wearable) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-12-17 |
| Device Publish Date | 2025-12-09 |
| 00815098021482 - Lifeline VIEW 2 | 2025-12-17 |
| 00815098021512 - Lifeline VIEW 2 Auto | 2025-12-17 |
| 00815098021536 - Lifeline ECG 2 | 2025-12-17 |
| 00815098021550 - DDU-29XX series, universal pad, single pair | 2025-12-17 |
| 10815098021496 - Lifeline VIEW 2 AED configuration | 2025-12-17 |
| 10815098021526 - Lifeline VIEW 2 AUTO AED configuration | 2025-12-17 |
| 10815098021540 - Lifeline ECG 2 AED configuration | 2025-12-17 |
| 30815098021568 - Pads, DDU-29XX series, universal pad, 10 pairs | 2025-12-17 |
| 30815098021568 - Pads, DDU-29XX series, universal pad, 10 pairs | 2025-12-17 |