Primary Device ID | 00889095040739 |
NIH Device Record Key | f489ecde-a5bf-4c97-9f3e-82a6ed88db50 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RELIEVE |
Version Model Number | 136.706 |
Company DUNS | 139105691 |
Company Name | GLOBUS MEDICAL, 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 | 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 | false |
OTC Over-The-Counter | false |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com | |
Phone | +1(610)930-1800 |
info@globusmedical.com |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Length | 6 Millimeter |
Outer Diameter | 2.6 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889095040739 [Primary] |
NQW | ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
[00889095040739]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-01 |
00889095040760 | RELIEVE 2.6mm Screw, Self-Tapping, 12mm |
00889095040753 | RELIEVE 2.6mm Screw, Self-Tapping, 10mm |
00889095040746 | RELIEVE 2.6mm Screw, Self-Tapping, 8mm |
00889095040739 | RELIEVE 2.6mm Screw, Self-Tapping, 6mm |
00889095040722 | RELIEVE 2.6mm Screw, Self-Tapping, 5mm |
00889095040715 | RELIEVE 2.6mm Screw, Self-Tapping, 4mm |
00889095040708 | RELIEVE 2.2mm Screw, Self-Tapping, 12mm |
00889095040692 | RELIEVE 2.2mm Screw, Self-Tapping, 10mm |
00889095040685 | RELIEVE 2.2mm Screw, Self-Tapping, 8mm |
00889095040678 | RELIEVE 2.2mm Screw, Self-Tapping, 6mm |
00889095040661 | RELIEVE 2.2mm Screw, Self-Tapping, 5mm |
00889095040654 | RELIEVE 2.2mm Screw, Self-Tapping, 4mm |
00889095040647 | RELIEVE 2.2mm Screw, Self-Drilling, 12mm |
00889095040630 | RELIEVE 2.2mm Screw, Self-Drilling, 10mm |
00889095040623 | RELIEVE 2.2mm Screw, Self-Drilling, 8mm |
00889095040616 | RELIEVE 2.2mm Screw, Self-Drilling, 6mm |
00889095040609 | RELIEVE 2.2mm Screw, Self-Drilling, 5mm |
00889095040593 | RELIEVE 2.2mm Screw, Self-Drilling, 4mm |
00889095215366 | RELIEVE Radiolucent Plate, Open Door, Widemouth, 13mm |
00889095215359 | RELIEVE Radiolucent Plate, Open Door, Widemouth, 11mm |
00889095215342 | RELIEVE Radiolucent Plate, Open Door, Widemouth, 9mm |
00889095215335 | RELIEVE Radiolucent Plate, Open Door, Widemouth, 7mm |
00889095215328 | RELIEVE Radiolucent Plate, Open Door, Widemouth, 5mm |
00889095215311 | RELIEVE Radiolucent Plate, Open Door, 13mm |
00889095215304 | RELIEVE Radiolucent Plate, Open Door, 11mm |
00889095215298 | RELIEVE Radiolucent Plate, Open Door, 9mm |
00889095215281 | RELIEVE Radiolucent Plate, Open Door, 7mm |
00889095215274 | RELIEVE Radiolucent Plate, Open Door, 5mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RELIEVE 97287918 not registered Live/Pending |
Laramy-K Optical, Inc. 2022-02-28 |
RELIEVE 97015236 not registered Live/Pending |
MEND Nutrition Inc. 2021-09-07 |
RELIEVE 88160260 not registered Dead/Abandoned |
SAVVY WELLNESS, INC. 2018-10-18 |
RELIEVE 78647809 not registered Dead/Abandoned |
Medtronic, Inc. 2005-06-10 |
RELIEVE 78592149 3178311 Live/Registered |
BOYD, DENNIS M 2005-03-22 |
RELIEVE 77953018 3927687 Dead/Cancelled |
Perrigo Florida, Inc. 2010-03-08 |
RELIEVE 77170793 3513357 Live/Registered |
Globus Medical, Inc. 2007-05-02 |
RELIEVE 75473728 not registered Dead/Abandoned |
Life Medical Sciences, Inc. 1998-04-24 |
RELIEVE 74661630 2005398 Dead/Cancelled |
Vesture Corporation 1995-04-17 |
RELIEVE 74647535 not registered Dead/Abandoned |
Pacific BioLogic, Inc. 1995-03-16 |
RELIEVE 74610114 not registered Dead/Abandoned |
CH2O International 1994-10-06 |
RELIEVE 73411424 1303412 Dead/Cancelled |
Johnson & Johnson 1983-01-28 |