Home GUDID 03663136006475 LUMIS™
Primary DI 03663136006475
Brand LUMIS™
Company SPINEVISION
Model MS1-A111
Device description PROTECTION SLEEVE FOR TAPS
Published 2015-10-21
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 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 03663136006475 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 03663136006475 03663136006475 3663136006475
GMDN Terms# Term, Definition table Term Definition Orthopaedic surgical procedure kit, non-medicated, reusable A collection of various orthopaedic surgical instruments, dressings and the necessary materials intended to be used to perform an orthopaedic surgical procedure, however the kit is not dedicated to orthopaedic implantation. It does not contain pharmaceuticals. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 390377518 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 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