| Primary Device ID | 30641043507357 |
| NIH Device Record Key | 2157008d-64e5-4df6-b628-1374c375215c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CPR Bag Reusable |
| Version Model Number | 10-50735 |
| Company DUNS | 032705659 |
| Company Name | MERCURY ENTERPRISES, 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 | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 30641043507357 [Primary] |
| BTM | Ventilator, Emergency, Manual (Resuscitator) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-31 |
| 30641043507357 | 10-50735 |
| 30641043507340 | 10-50734 |
| 30641043507333 | 10-50733 |
| 30641043507326 | 10-50732 |
| 30641043507319 | 10-50731 |
| 30641043507241 | 10-50724 |
| 30641043507197 | 10-50719 |
| 30641043507180 | 10-50718 |
| 30641043507173 | 10-50717 |
| 30641043507166 | 10-50716 |
| 30641043507074 | 10-50707 |
| 30641043507067 | 10-50706 |
| 30641043507050 | 10-50705 |
| 30641043507043 | 10-50704 |
| 30641043507029 | 10-50702 |
| 30641043507012 | 10-50701 |
| 30641043507005 | 10-50700 |