Primary Device ID | 00815871022323 |
NIH Device Record Key | e5e6ae3b-dcba-43ad-baed-783cd4b1d4de |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vista LED |
Version Model Number | DRE 061322 |
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 | 00815871022323 [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 |