Home GUDID 08809974819906 AnyPlus Spinal Fixation System
Primary DI 08809974819906
Brand AnyPlus Spinal Fixation System
Company GS Medical Co., Ltd.
Model 2503-0065
Catalog number 2503-0065
Device description A small, threaded, implantable rod with a screw head and drive intended for internal spinal fixation by being screwed into the spine to hold a correction/stabilization device (e.g., rod, plate, tether) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (e.g., surgical steel, titanium alloy, carbon fibre). It is available in various types (e.g., pedicle or transfacet, with a slotted, cross, star, or polygonal drive), and is typically used to provide immobilization and stabilization of spinal segments in the treatment of spinal instabilities or deformities. A screw head adaptor intended to stabilize a rod may be included with the screw.
Published 2026-11-03
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false
Product Codes# Code, Name table Code Name KWP Appliance, Fixation, Spinal Interlaminal KWQ Appliance, Fixation, Spinal Intervertebral Body NKB Thoracolumbosacral Pedicle Screw System
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 NKB Thoracolumbosacral Pedicle Screw System Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 08809974819906 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 08809974819906 08809974819906 8809974819906
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 688385418 Device count 1 DM exempt true Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number true Manufacturing date on label true Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 08800322693902 VEGA Cervical Screw System 1440-0025 1440-0025 2026-11-03 08800322693919 VEGA Cervical Screw System 1440-0025-M0 1440-0025-M0 2026-11-03 08800322693926 VEGA Cervical Screw System 1440-0030 1440-0030 2026-11-03 08800322693933 VEGA Cervical Screw System 1440-0030-M0 1440-0030-M0 2026-11-03 08800322693940 VEGA Cervical Screw System 1440-0035 1440-0035 2026-11-03 08800322693957 VEGA Cervical Screw System 1440-0035-M0 1440-0035-M0 2026-11-03 08800322693964 VEGA Cervical Screw System 1440-0040 1440-0040 2026-11-03 08800322693971 VEGA Cervical Screw System 1440-0040-M0 1440-0040-M0 2026-11-03 08800322693988 VEGA Cervical Screw System 1440-0045 1440-0045 2026-11-03 08800322693995 VEGA Cervical Screw System 1440-0045-M0 1440-0045-M0 2026-11-03 08800322694008 VEGA Cervical Screw System 1440-0050 1440-0050 2026-11-03 08800322694015 VEGA Cervical Screw System 1440-0050-M0 1440-0050-M0 2026-11-03 08800322694022 VEGA Cervical Screw System 1440-0055 1440-0055 2026-11-03 08800322694039 VEGA Cervical Screw System 1440-0055-M0 1440-0055-M0 2026-11-03 08800322694046 VEGA Cervical Screw System 1440-0060 1440-0060 2026-11-03 08800322694053 VEGA Cervical Screw System 1440-0060-M0 1440-0060-M0 2026-11-03 08800322694060 VEGA Cervical Screw System 1440-0065 1440-0065 2026-11-03 08800322694077 VEGA Cervical Screw System 1440-0065-M0 1440-0065-M0 2026-11-03 08800322694084 VEGA Cervical Screw System 1440-0070 1440-0070 2026-11-03 08800322694091 VEGA Cervical Screw System 1440-0070-M0 1440-0070-M0 2026-11-03
Other Devices Sharing Product Codes#