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 |