Home GUDID 00889024323742
ST360°®
Primary DI 00889024323742
Brand ST360°®
Company ZIMMER SPINE, INC.
Model 07.00443.001
Catalog number 07.00443.001
Published 2016-06-22
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 KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL MNH Orthosis, spondylolisthesis spinal fixation MNI ORTHOSIS, SPINAL PEDICLE FIXATION NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2 MNH Orthosis, Spondylolisthesis Spinal Fixation Orthopedic 2 MNI Orthosis, Spinal Pedicle Fixation Orthopedic 2 NKB Thoracolumbosacral Pedicle Screw System Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00889024323742 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 00889024323742 00889024323742 889024323742 0889024323742
GMDN Terms# Term, Definition table Term Definition General internal orthopaedic fixation system implantation kit A collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 787663400 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