| Primary Device ID | 30641043553514 |
| NIH Device Record Key | ed33b2bc-ead7-46d5-b219-bd8f455f0b58 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Manometer |
| Version Model Number | 10-55351 |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10641043553510 [Primary] |
| GS1 | 30641043553514 [Package] Contains: 10641043553510 Package: [12 Units] In Commercial Distribution |
| CAP | Monitor, Airway Pressure (Includes Gauge And/Or Alarm) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-04-09 |
| Device Publish Date | 2016-05-06 |
| 30641043553507 | 10-55350 |
| 30641043553828 | 10-55382 |
| 30641043553811 | 10-55381 |
| 30641043553798 | 10-55379 |
| 30641043553781 | 10-55378 |
| 30641043553774 | 10-55377 |
| 30641043553675 | 10-55367 |
| 10641043553664 | 10-55366 |
| 30641043553651 | 10-55365 |
| 30641043553644 | 10-55364 |
| 30641043553590 | 10-55359 |
| 10641043553589 | 10-55358 |
| 30641043553576 | 10-55357 |
| 30641043553569 | 10-55356 |
| 30641043553545 | 10-55354 |
| 30641043553538 | 10-55353 |
| 30641043553521 | 10-55352 |
| 30641043553514 | 10-55351 |