| Primary Device ID | 10815098020512 |
| NIH Device Record Key | f1bc7ca2-a9b3-4710-9ae9-912820e5a2eb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DDU-2XXX Series ECGMA Cable, AAMI Configuration |
| Version Model Number | DAC-2020 |
| 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 | 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10815098020512 [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 | 4 |
| Public Version Date | 2024-06-06 |
| Device Publish Date | 2015-10-24 |
| 10815098020475 - DDU-1XX Series Adult Pads Adapter, Physio-Control Configuration | 2024-06-06 |
| 10815098020482 - DDU-1XX Series Adult Pads Adapter, Zoll Configuration | 2024-06-06 |
| 10815098020499 - DDU-1XXX/2XXX Adult Pads Adapter, Physio-Control Configuration | 2024-06-06 |
| 10815098020505 - DDU-1XXX/2XXX Adult Pads Adapter, Zoll Configuration | 2024-06-06 |
| 10815098020512 - DDU-2XXX Series ECGMA Cable, AAMI Configuration | 2024-06-06 |
| 10815098020512 - DDU-2XXX Series ECGMA Cable, AAMI Configuration | 2024-06-06 |
| 10815098020529 - DDU-2XXX Series ECGMA Cable, IEC Configuration | 2024-06-06 |
| 10815098020437 - DDU-1XX Series Pediatric Pads Configuration | 2023-07-06 |
| 10815098020451 - DDU-1XXX/2XXX Series Pediatric Pads Configuration | 2023-07-06 |