| Primary Device ID | 30641043566033 |
| NIH Device Record Key | 9175990c-8bd8-4009-9a0f-73226186f2d7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CPR-2 Bag |
| Version Model Number | 10-56603 |
| Company DUNS | 032705659 |
| Company Name | MERCURY ENTERPRISES, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com | |
| Phone | (727) 573-0088 |
| hospitalcustomerservice@mercurymed.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10641043566039 [Primary] |
| GS1 | 30641043566033 [Package] Contains: 10641043566039 Package: [6 Units] In Commercial Distribution |
| BTM | Ventilator, Emergency, Manual (Resuscitator) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-23 |
| Device Publish Date | 2025-07-15 |