| Primary Device ID | 00883873940204 |
| NIH Device Record Key | 8fc666ff-968e-462f-984b-ffdaeb60d315 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 11140 |
| Catalog Number | 11140-000072 |
| Company DUNS | 009251992 |
| Company Name | PHYSIO-CONTROL, INC. |
| 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 | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00883873940204 [Primary] |
| MPD | Auxiliary power supply (AC or DC) for low-energy dc-defibrillator |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-05-08 |
| Device Publish Date | 2019-04-30 |