| Primary Device ID | 07290013818829 |
| NIH Device Record Key | 6c0163ca-d185-49dd-ade2-cbf11b29a4ba |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Natus |
| Version Model Number | NA-1340 |
| Company DUNS | 023572393 |
| Company Name | SLP 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 | false |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290013818829 [Primary] |
| MNR | Ventilatory Effort Recorder |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-20 |
| 07290013820167 | NA-1475-Kit |
| 07290013818843 | NA-1550 |
| 07290013818836 | NA-1341 |
| 07290013818829 | NA-1340 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NATUS 87624187 5453399 Live/Registered |
Natus Medical Incorporated 2017-09-27 |
![]() NATUS 86540434 4812806 Live/Registered |
Natus Medical Incorporated 2015-02-19 |
![]() NATUS 85893616 not registered Dead/Abandoned |
Lestat, Ofel 2013-04-03 |
![]() NATUS 85653367 not registered Dead/Abandoned |
RagTrade Industries, LLC 2012-06-15 |
![]() NATUS 85437060 4153501 Live/Registered |
Natus Medical Incorporated 2011-09-30 |
![]() NATUS 74073532 1637520 Live/Registered |
Natus Medical Inc. 1990-06-28 |
![]() NATUS 73834858 1635226 Dead/Cancelled |
NATUS CORPORATION 1989-10-30 |