| Primary Device ID | 00815871022361 |
| NIH Device Record Key | 8c0b68b1-33af-4c11-aaca-350fe51c243a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vista LED |
| Version Model Number | DRE 061322-V |
| Company DUNS | 178440426 |
| Company Name | Avante |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 00815871022361 [Primary] |
| KZF | Device, Medical Examination, Ac Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2017-02-01 |
| 00815871022392 | DRE Vista LED, DC |
| 00815871022385 | DRE Vista LED, SINGLE CEILING |
| 00815871022378 | DRE Vista LED, FLOOR |
| 00815871022361 | DRE Vista LED, WALL |
| 00815871022354 | DRE Vista LED, DC |
| 00815871022347 | DRE Vista LED, SINGLE CEILING |
| 00815871022330 | DRE Vista LED, FLOOR |
| 00815871022323 | DRE Vista LED, WALL |
| 00815871021876 | DRE Vista LED, DC |
| 00815871021869 | DRE Vista LED, SINGLE CEILING |
| 00815871021852 | DRE Vista LED, FLOOR |
| 00815871021845 | DRE Vista LED, WALL |
| 00815871021838 | DRE Vista LED, DC |
| 00815871021821 | DRE Vista LED, SINGLE CEILING |
| 00815871021814 | DRE Vista LED, FLOOR |
| 00815871021807 | DRE Vista LED, WALL |