| Primary Device ID | 00721902381768 |
| NIH Device Record Key | af281df4-4fd7-494c-ba21-5f65a14f36f7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ELECTRODE ASSY-QUIK-COMBO |
| Version Model Number | 11103 |
| Catalog Number | 11103-000023 |
| Company DUNS | 009251992 |
| Company Name | PHYSIO-CONTROL, 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00721902381768 [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 | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2014-11-10 |
| 00721902381768 | ELECTRODE ASSY-QUIK-COMBO QUIK-PAK,SET,WW |
| 00883873824610 | ELECTRODE ASSY-QUIK-COMBO QUIK-PAK,SET,WW |