| Primary Device ID | 00883873948323 |
| NIH Device Record Key | 3acb24e9-ed68-43f7-8dcf-28fa2a5ef6dd |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 11576 |
| Catalog Number | 11576-000060 |
| Company DUNS | 632662933 |
| Company Name | Jolife AB |
| 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 | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00883873948323 [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 | 2020-02-06 |
| Device Publish Date | 2019-04-30 |
| 00883873881453 - NA | 2020-02-06 LUCAS POWER SUPPLY WITHCORD,REDEL,CANADA,US |
| 00883873948323 - NA | 2020-02-06LUCAS BATTERY CHARGER,MAINS PLUG,US-CAN-JA |
| 00883873948323 - NA | 2020-02-06 LUCAS BATTERY CHARGER,MAINS PLUG,US-CAN-JA |
| 00883873861820 - LUCAS CHEST COMPRESSION SYSTEM | 2018-10-31 LUCAS BATTERY DARK GRAY |
| 00883873834329 - LUCAS | 2018-10-05 LUCAS 3, 3.1, IN SHIPPING BOX, EN |
| 00883873861875 - LUCAS™ CHEST COMPRESSION SYSTEM | 2018-03-29 LUCAS 3, 3.0, IN SHIPPING BOX, EN |
| 00883873904565 - LUCAS™ Chest Compression System | 2018-03-29 LUCAS 2, 2.2, IN SHIPPING BOX,EN |
| 00883873948286 - Lucas PCI Back Plate | 2018-03-29 LUCAS PCI BACK PLATE |
| 00883873970898 - Lucas Battery Pack | 2018-03-29 LUCAS 2 BATTERY |