Home GUDID M711E3U65350 Excella III-D®
Primary DI M711E3U65350
Brand Excella III-D®
Company INNO Holdings, Inc.
Model E3U6535
Catalog number E3U6535
Device description Ti 6Al 4V (ELI)
Published 2015-12-31
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true Product Codes# Code, Name table Code Name KWP Appliance, Fixation, Spinal Interlaminal KWQ Appliance, Fixation, Spinal Intervertebral Body 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 KWQ Appliance, Fixation, Spinal Intervertebral Body 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 M711E3U65350 Primary HIBCC 0
GMDN Terms# Term, Definition table Term Definition Spinal bone screw, non-bioabsorbable A small, threaded, implantable rod with a slotted head intended to be used for internal spinal fixation by being screwed into the spine to hold a correction/stabilization device (e.g., rod, plate, tether) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is available in various types, including pedicle and transfacet, and is typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities.
Device Sizes# Type, Value, Unit table Type Value Unit Length 35 Millimeter Outer Diameter 6.5 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 141620464 Device count 1 DM exempt true 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 00840466901011 Primus SPINAL ELEMENTS, INC. KWP 2026-10-22 00840466901011 Primus SPINAL ELEMENTS, INC. NKB 2026-10-22 00840466901011 Primus SPINAL ELEMENTS, INC. KWQ 2026-10-22 00840606168472 SAPPHIRE X SPINAL ELEMENTS, INC. KWQ 2026-10-22 00840606168502 SAPPHIRE X SPINAL ELEMENTS, INC. KWQ 2026-10-22 00840606174855 Primus SPINAL ELEMENTS, INC. NKB 2026-10-22 00840606175142 Primus SPINAL ELEMENTS, INC. NKB 2026-10-22 00840606175203 Primus SPINAL ELEMENTS, INC. NKB 2026-10-22 00840606185868 Primus SPINAL ELEMENTS, INC. NKB 2026-10-22 03701313009823 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009830 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009854 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009878 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009885 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009892 KHEIRON S.M.A.I.O NKB 2026-10-22 03701313009908 KHEIRON S.M.A.I.O NKB 2026-10-22 00197157123611 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157123628 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157123635 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157123642 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157123659 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157123666 ZAVATION SCREW Zavation LLC NKB 2026-10-21 00197157122874 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122881 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122898 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122904 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122911 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122928 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122935 ZAVATION SCREW Zavation LLC NKB 2026-10-20 00197157122942 ZAVATION SCREW Zavation LLC NKB 2026-10-20