Home GUDID 00841193103099
nuMIS Lumbar Plating System
Primary DI 00841193103099
Brand nuMIS Lumbar Plating System
Company Cutting Edge Spine, LLC
Model 27161
Catalog number 27161
Device description nuMIS™ Long Hex Driver
Published 2015-10-30
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Product Codes# Code, Name table Code Name MNH Orthosis, spondylolisthesis spinal fixation MNI ORTHOSIS, SPINAL PEDICLE FIXATION
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
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00841193103099 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 00841193103099 00841193103099 841193103099 0841193103099
GMDN Terms# Term, Definition table Term Definition Surgical screwdriver, reusable A non-powered tool intended to fit into a screw head (e.g., slotted, cross/hex head) for the application of rotation to introduce/remove a screw (e.g., craniofacial bone screw, dental screw) into/from a patient in association with a surgical procedure [e.g., orthopaedic, dental, computer assisted surgery (CAS), image registration]. It may also be used to connect/disconnect a device to/from another device attached to a patient (e.g., implant component, fiducial marker). The proximal end of the device may have a handle for manual use or a profiled tang that fits into an independent chuck or power driver; it is typically made of metallic and/or polymer materials. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Length 12 Inch
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 Store at room temperature
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 069472647 Device count 1 DM exempt true Lot or batch true Manufacturing date on label true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00841193127996 T-FIX™3Dsi Joint Fusion System CES-643 2026-03-24 00841193127521 EVOL®ha-Hyper C Cervical Interbody System 6012-0507A 6012-0507A 2026-03-11 00841193127538 EVOL®ha-Hyper C Cervical Interbody System 6012-0607A 6012-0607A 2026-03-11 00841193127545 EVOL®ha-Hyper C Cervical Interbody System 6012-0707A 6012-0707A 2026-03-11 00841193127552 EVOL®ha-Hyper C Cervical Interbody System 6012-0807A 6012-0807A 2026-03-11 00841193127569 EVOL®ha-Hyper C Cervical Interbody System 6012-0907A 6012-0907A 2026-03-11 00841193127576 EVOL®ha-Hyper C Cervical Interbody System 6012-1007A 6012-1007A 2026-03-11 00841193127583 EVOL®ha-Hyper C Cervical Interbody System 6012-1107A 6012-1107A 2026-03-11 00841193127590 EVOL®ha-Hyper C Cervical Interbody System 6012-1207A 6012-1207A 2026-03-11 00841193127606 EVOL®ha-Hyper C Cervical Interbody System 6013-0512A 6013-0512A 2026-03-11 00841193127613 EVOL®ha-Hyper C Cervical Interbody System 6013-0612A 6013-0612A 2026-03-11 00841193127620 EVOL®ha-Hyper C Cervical Interbody System 6013-0712A 6013-0712A 2026-03-11 00841193127637 EVOL®ha-Hyper C Cervical Interbody System 6013-0812A 6013-0712A 2026-03-11 00841193127644 EVOL®ha-Hyper C Cervical Interbody System 6013-0912A 6013-0912A 2026-03-11 00841193127651 EVOL®ha-Hyper C Cervical Interbody System 6013-1012A 6013-1012A 2026-03-11 00841193127668 EVOL®ha-Hyper C Cervical Interbody System 6013-1112A 6013-1112A 2026-03-11 00841193127675 EVOL®ha-Hyper C Cervical Interbody System 6013-1212A 6013-1212A 2026-03-11 00841193101934 EVOS Lumbar Interbody System 4014-016 4014-016 2015-10-30 00841193104836 EVOS Lumbar Interbody System 4067-010 4067-010 2015-10-30 00841193105635 EVOS Lumbar Interbody System 4004-014 4004-014 2016-01-12
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