Home GUDID 10889981303310
Specials
Primary DI 10889981303310
Brand Specials
Company Seaspine Orthopedics Corporation
Model SR-0929
Catalog number SR-0929
Device description Extended Shank Driver Sleeve
Published 2022-08-25
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 KWQ Appliance, fixation, spinal intervertebral body MNH Orthosis, spondylolisthesis spinal fixation MNI Orthosis, spinal pedicle fixation NKB Thoracolumbosacral pedicle screw system
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class 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 10889981303310 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10889981303310 10889981303310
GMDN Terms# Term, Definition table Term Definition Orthopaedic implantation sleeve, reusable A hand-held tubular surgical device designed to be used during an orthopaedic implantation procedure to hold/grip an implant (e.g., an orthopaedic bone screw), facilitate the acceptance of an orthopaedic instrument (e.g., a screwdriver or a smaller diameter sleeve) through it, stabilize an instrument/implant coupling, and/or protect the surgeon's gloved hand or patient tissue. It is not primarily intended to place, angle, and guide a rotating surgical drill. It is typically made of high-grade stainless steel and/or synthetic materials and is available in various sizes and lengths. This is a reusable device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 079840876 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 08800043949180 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965029 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965036 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965043 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965050 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965067 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965074 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965081 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965098 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965104 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965111 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965128 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965135 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965142 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965159 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965166 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965173 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965180 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965197 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965203 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965210 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965227 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965234 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965241 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965258 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965265 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965272 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965289 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965296 N/A TDM Co., Ltd. KWQ 2026-06-05 08800043965302 N/A TDM Co., Ltd. KWQ 2026-06-05