Home GUDID 07640139342133
ROMEO 2 INSTRUMENTATION
Primary DI 07640139342133
Brand ROMEO 2 INSTRUMENTATION
Company SpineArt SA
Model ELL-IN 00 15-N
Catalog number ELL-IN 00 15-N
Device description Guide nut
Published 2016-09-27
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
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
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 07640139342133 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07640139342133 07640139342133 7640139342133
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 483016148 Device count 1 Lot or batch true Manufacturing date on label 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 00840466901035 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901042 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901059 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901066 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901073 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901080 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901097 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901103 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901110 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901127 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901141 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901158 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901165 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901172 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901479 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901486 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901493 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901509 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901516 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901523 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901530 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901547 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901554 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901561 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901578 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901585 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901592 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901608 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901615 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901622 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21