Primary Device ID | 00815871021722 |
NIH Device Record Key | d8ccf684-d58c-4972-9591-4e95fa813d4e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VISION EX5 |
Version Model Number | DRE 061412 |
Company DUNS | 178440426 |
Company Name | Avante |
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 | 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 | 00815871021722 [Primary] |
FST | Light, Surgical, Fiberoptic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2016-09-23 |
00815871022453 | DRE Vision EX5, FLOOR MODEL, BATTERY BACKUP |
00815871022446 | DRE Vision EX5, FLOOR MODEL, BATTERY BACKUP |
00815871022316 | DRE Vision EX5, DUAL CEILING |
00815871022309 | DRE Vision EX5, SINGLE CEILING |
00815871022293 | DRE Vision EX5, FLOOR MODEL |
00815871022286 | DRE Vision EX5, WALL MOUNT |
00815871022279 | DRE Vision EX5, DUAL CEILING |
00815871022262 | DRE Vision EX5, SINGLE CEILING |
00815871022255 | DRE Vision EX5, FLOOR MODEL |
00815871022248 | DRE Vision EX5, WALL MOUNT |
00815871021791 | DRE Vision EX5, DUAL CEILING |
00815871021784 | DRE Vision EX5, SINGLE CEILING |
00815871021777 | DRE Vision EX5, FLOOR MODEL |
00815871021760 | DRE Vision EX5, DUAL CEILING |
00815871021753 | DRE Vision EX5, DUAL CEILING |
00815871021746 | DRE Vision EX5, SINGLE CEILING |
00815871021739 | DRE Vision EX5, FLOOR MODEL |
00815871021722 | DRE Vision EX5, WALL MOUNT |