Home GUDID 10889981070526
Mariner
Primary DI 10889981070526
Brand Mariner
Company Seaspine Orthopedics Corporation
Model 41-9535-2
Catalog number 41-9535-2
Device description Cannulated Screw 9.50 x 35mm
Published 2016-09-02
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 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 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 10889981070526 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10889981070526 10889981070526
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system, non-sterile An assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included.
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 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