| Primary Device ID | 00818089021256 |
| NIH Device Record Key | f4db16fb-5a4b-4145-96f7-9892918061d3 |
| Commercial Distribution Discontinuation | 2022-08-03 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | LifeVue |
| Version Model Number | 90X0531 |
| Company DUNS | 081712583 |
| Company Name | Nds Surgical Imaging LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 | 00818089021256 [Primary] |
| KQM | Camera, Surgical And Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-08-11 |
| Device Publish Date | 2022-08-03 |
| 00818089021256 | LIFEVUE 19", WALLMOUNT, W/TOUCH, CUSTOM KARL STORZ US, V3C-SX19-R130 |
| 00818089021249 | LIFEVUE 19", W/ DESKTOP STAND, W/TOUCH, CUSTOM KARL STORZ, V3C-SX19-R110 |
| 00851455007959 | CRYOCATH, 15" LIFEVUE, V3C-X15-R210, |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LIFEVUE 90323495 not registered Live/Pending |
Allegis Group, Inc. 2020-11-17 |
![]() LIFEVUE 85152598 3973993 Dead/Cancelled |
Cynergi Systems, LLC 2010-10-14 |