Primary Device ID | 03663136007212 |
NIH Device Record Key | 49c059df-bddc-4c26-8dcb-7742c8153e74 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LUMIS™ |
Version Model Number | MS1-R6055T |
Company DUNS | 390377518 |
Company Name | SPINEVISION |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03663136007212 [Primary] |
MNH | Orthosis, spondylolisthesis spinal fixation |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
[03663136007212]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2025-01-17 |
Device Publish Date | 2015-10-15 |
03663136020181 | Ti 6.0 mm x 135 mm PRE-BENT PERCUTANEOUS ROD |
03663136018782 | Ø8mm CANNULATED TAP |
03663136007809 | MULTI-AXIAL SCREW Ø 8.5mm L 60mm |
03663136007670 | MULTI-AXIAL SCREW Ø 6.5mm L 55mm |
03663136006949 | MULTI-AXIAL SCREW, DIAMETER 5.5mm, LENGTH 45mm |
03663136006925 | MULTI-AXIAL SCREW, DIAMETER 5.5mm, LENGTH 35mm |
03663136007793 | MULTI-AXIAL SCREW Ø 8.5mm L 55mm |
03663136007724 | MULTI-AXIAL SCREW Ø 7.5mm L 50mm |
03663136007595 | MULTI-AXIAL SCREW Ø 5.5mm L 45mm |
03663136007540 | GUIDE WIRE DIAMETER 1.4mm, LENGTH 500mm |
03663136007366 | Ti 6.0 mm x 100 mm PRE-BENT PERCUTANEOUS ROD |
03663136007335 | Ti 6.0 mm x 85 mm STRAIGHT PERCUTANEOUS ROD |
03663136007274 | Ti 6.0 mm x 70 mm STRAIGHT PERCUTANEOUS ROD |
03663136006987 | MULTI-AXIAL SCREW, DIAMETER 6.5mm, LENGTH 40mm |
03663136006628 | INDEX RING FOR SETSCREW HOLDER |
03663136006611 | SETSCREW HOLDER |
03663136007755 | MULTI-AXIAL SCREW Ø 8.5mm L35mm |
03663136027654 | Prebent percutaneous rod 6.0mm x 35mm |
03663136027647 | Prebent percutaneous rod 6.0mm x 30mm |
03663136027630 | Straight percutaneous rod 6.0mm x 35mm |
03663136027623 | Straight percutaneous rod 6.0mm x 30mm |
03663136023670 | LUMIS™ INSERT FOR INSTRUMENTS |
03663136020174 | Ti 6.0 mm x 125 mm PRE-BENT PERCUTANEOUS ROD |
03663136020167 | Ti 6.0 mm x 115 mm PRE-BENT PERCUTANEOUS ROD |
03663136020150 | Ti 6.0 mm x 105 mm PRE-BENT PERCUTANEOUS ROD |
03663136020143 | Ti 6.0 mm x 95 mm PRE-BENT PERCUTANEOUS ROD |
03663136020136 | Ti 6.0 mm x 135 mm STRAIGHT PERCUTANEOUS ROD |
03663136020129 | Ti 6.0 mm x 125 mm STRAIGHT PERCUTANEOUS ROD |
03663136020112 | Ti 6.0 mm x 115 mm STRAIGHT PERCUTANEOUS ROD |
03663136020105 | Ti 6.0 mm x 105 mm STRAIGHT PERCUTANEOUS ROD |
03663136020099 | Ti 6.0 mm x 95 mm STRAIGHT PERCUTANEOUS ROD |
03663136020082 | MULTI-AXIAL SCREW, DIAMETER 6.5mm, LENGTH 60mm |
03663136008172 | MOFALSEBLOC SCREW, Ø 8.5mm, L 90mm |
03663136008165 | MOFALSEBLOC SCREW, Ø 8.5mm, L 85mm |
03663136008158 | MOFALSEBLOC SCREW, Ø 8.5mm, L 80mm |
03663136008141 | MOFALSEBLOC SCREW, Ø 8.5mm, L 75mm |
03663136008103 | MOFALSEBLOC SCREW, Ø 8.5mm, L 55mm |
03663136008097 | MOFALSEBLOC SCREW, Ø 8.5mm, L 50mm |
03663136008073 | MOFALSEBLOC SCREW, Ø 8.5mm, L 40mm |
03663136008066 | MOFALSEBLOC SCREW, Ø 8.5mm, L 35mm |
03663136008059 | MOFALSEBLOC SCREW, Ø 7.5mm, L 60mm |
03663136008042 | MOFALSEBLOC SCREW, Ø 7.5mm, L 55mm |
03663136008035 | LUMIS™MOFALSEBLOC SCREW, Ø 7.5mm, L 50mm |
03663136008028 | MOFALSEBLOC SCREW, Ø 7.5mm, L 45mm |
03663136008011 | MOFALSEBLOC SCREW, Ø 7.5mm, L 40mm |
03663136007991 | MOFALSEBLOC SCREW, Ø 6.5mm, L 60mm |
03663136007984 | MOFALSEBLOC SCREW, Ø 6.5mm, L 55mm |
03663136007977 | MOFALSEBLOC SCREW, Ø 6.5mm, L 50mm |
03663136007960 | MOFALSEBLOC SCREW, Ø 6.5mm, L 45mm |
03663136007953 | MOFALSEBLOC SCREW, Ø 6.5mm, L 40mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() LUMIS 98749003 not registered Live/Pending |
JV Eighteen LLC 2024-09-13 |
![]() LUMIS 98497161 not registered Live/Pending |
Jekabs Otankis 2024-04-12 |
![]() LUMIS 97723392 not registered Live/Pending |
Lumis Corp 2022-12-19 |
![]() LUMIS 90252344 not registered Live/Pending |
Lumis Group LLC 2020-10-13 |
![]() LUMIS 90252294 not registered Live/Pending |
Lumis Group LLC 2020-10-13 |
![]() LUMIS 87870684 not registered Live/Pending |
SS&C Technologies, Inc. 2018-04-10 |
![]() LUMIS 86139443 4697031 Live/Registered |
RESMED PTY LTD 2013-12-10 |
![]() LUMIS 85719352 not registered Dead/Abandoned |
LUMINATION LLC 2012-09-03 |
![]() LUMIS 79092308 4047593 Live/Registered |
Spinevision 2010-12-03 |
![]() LUMIS 76245075 not registered Dead/Abandoned |
BRISTOL-MYERS SQUIBB PHARMA COMPANY 2001-04-23 |
![]() LUMIS 75677267 not registered Dead/Abandoned |
McCullough, William 1999-04-10 |