Home GUDID 00817329025900
ModuLIF
Primary DI 00817329025900
Brand ModuLIF
Company LINKSPINE, INC.
Model 80-4900
Catalog number 80-4900
Device description ModuLIF Set
Published 2018-08-09
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Product Codes# Code, Name table Code Name MNH Orthosis, Spondylolisthesis Spinal Fixation MNI Orthosis, Spinal Pedicle Fixation MRW System, Facet Screw Spinal Device NKB Thoracolumbosacral Pedicle Screw System
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MNH Orthosis, Spondylolisthesis Spinal Fixation Orthopedic 2 MNI Orthosis, Spinal Pedicle Fixation Orthopedic 2 MRW System, Facet Screw Spinal Device Unknown U NKB Thoracolumbosacral Pedicle Screw System Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00817329025900 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 00817329025900 00817329025900 817329025900 0817329025900
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system, non-sterile An assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 067584601 Device count 1 Lot or batch true 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 B678520297S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520297S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520297S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520298S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520298S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520298S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520299S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520299S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520299S0 PressON NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520300S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520300S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520300S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520301S0 PressON NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520301S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520301S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520302S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520302S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520302S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520303S0 PressON NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520303S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520303S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520304S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520304S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520304S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520305S0 PressON NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520305S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520305S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520306S0 PressON™ NEXUS SPINE, L.L.C. NKB 2026-07-10 B678520306S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520306S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10