Primary Device ID | 01816835023089 |
NIH Device Record Key | 2aa3611d-da63-4855-ad94-e1ad7cc2e30c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vu-E |
Version Model Number | NVSD3CD3-E-LCH |
Company DUNS | 093357739 |
Company Name | MEDICAL ILLUMINATION INTERNATIONAL 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 | true |
Manufacturing Date | true |
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 | 00816835023080 [Primary] |
GS1 | 01816835023089 [Package] Contains: 00816835023080 Package: BOX [1 Units] In Commercial Distribution |
FST | Light, Surgical, Fiberoptic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-24 |
Device Publish Date | 2020-03-16 |
01816835023140 | Vu-E, DUAL, SURGICAL LIGHT W/MONITOR ARM |
01816835023133 | Vu-E, SOLO, SURGICAL LIGHT |
01816835023126 | Vu-E, TRIO, SURGICAL LIGHTS, W/MONITOR ARM |
01816835023119 | Vu-E, DUAL, SURGICAL LIGHTS |
01816835023102 | Vu-E, SOLO, IL-CR SURGICAL LIGHT |
01816835023096 | Vu-E, TRIO,IL-CR SURGICAL LIGHT, SURGICAL LIGHT, W/MONITOR ARM |
01816835023089 | Vu-E, DUAL, IL-CR SURGICAL LIGHT & SURGICAL LIGHT |
01816835023898 | Vu-E, TRIO, SURGICAL LGHT W/MONITOR ARM |