Home GUDID 00190837085728 ProLift Lateral
Primary DI 00190837085728
Brand ProLift Lateral
Company Life Spine, Inc.
Model 149-4002
Catalog number 149-4002
Device description Graft Cannula Tamp
Published 2019-11-19
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name MAX Intervertebral fusion device with bone graft, lumbar
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00190837085728 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00190837085728 00190837085728 190837085728 0190837085728
GMDN Terms# Term, Definition table Term Definition Bone graft delivery kit A collection of sterile devices intended to be used to prepare and/or deliver bone graft material during an orthopaedic surgical procedure. It typically includes aspirating/delivery/mixing syringe(s), an adaptor, and a needle/cannula. It allows for the aspiration and/or premixing of bone marrow, autologous blood, plasma, intravenous fluids (IVF), and bone void filler (e.g., allograft, autograft, synthetic bone graft material), and their delivery to the surgical site. This is a single-use device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 183641617 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00840606185110 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606185127 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606185134 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606185141 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606185158 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606185165 LUNA Ti SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606196024 Vertu SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606196031 Vertu SPINAL ELEMENTS, INC. MAX 2026-09-25 00840606196048 Vertu SPINAL ELEMENTS, INC. MAX 2026-09-25 00810017915170 SABER-XA, Screw Ø5.5 x 32.5 ELEVATION SPINE, INC. MAX 2026-09-22 10888857461819 CASCADIA™ Interbody System VB Spine LLC MAX 2019-10-31 10888857461888 CASCADIA™ Interbody System VB Spine LLC MAX 2019-10-31 04546540665720 AVS NAVIGATOR Stryker Corporation MAX 2016-09-24 10888857218772 CASCADIA™ Interbody System VB Spine LLC MAX 2015-12-16 10888857218963 CASCADIA™ Interbody System VB Spine LLC MAX 2015-12-16 10888857219076 CASCADIA™ Interbody System VB Spine LLC MAX 2015-12-16 10888857219489 CASCADIA™ Interbody System VB Spine LLC MAX 2015-12-16 10888857219595 CASCADIA™ Interbody System VB Spine LLC MAX 2015-12-16 07613153046196 AVS PL Stryker Corporation MAX 2015-09-14 07613153046202 AVS PL Stryker Corporation MAX 2015-09-14 07613153046219 AVS PL Stryker Corporation MAX 2015-09-14 07613153046226 AVS PL Stryker Corporation MAX 2015-09-14 07613153046233 AVS PL Stryker Corporation MAX 2015-09-14 07613153046288 AVS PL Stryker Corporation MAX 2015-09-14 07613153046295 AVS PL Stryker Corporation MAX 2015-09-14 07613153046301 AVS PL Stryker Corporation MAX 2015-09-14 07613153046318 AVS PL Stryker Corporation MAX 2015-09-14 07613153046325 AVS PL Stryker Corporation MAX 2015-09-14 07613153046332 AVS PL Stryker Corporation MAX 2015-09-14 07613153046349 AVS PL Stryker Corporation MAX 2015-09-14