Home GUDID 08806373836282 LOSPA IS Spinal System
Primary DI 08806373836282
Brand LOSPA IS Spinal System
Company Corentec Co., Ltd
Model 01.26.863
Device description Pedicle screw(Guided, Anodizing)
Published 2015-10-20
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
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
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 08806373836282 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 08806373836282 08806373836282 8806373836282
GMDN Terms# Term, Definition table Term Definition Spinal bone screw, non-bioabsorbable A small, threaded, implantable rod with a slotted head intended to be used 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 (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is available in various types, including pedicle and transfacet, and is typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 688739895 Device count 1 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 08800017262925 EXULT Knee Replacement System K3.IBN.4266-12T 2020-01-10 08800017262932 EXULT Knee Replacement System K3.IBN.4266-13T 2020-01-10 08800017262949 EXULT Knee Replacement System K3.IBN.4266-14T 2020-01-10 08800017262956 EXULT Knee Replacement System K3.IBN.4266-16T 2020-01-10 08800017262963 EXULT Knee Replacement System K3.IBN.4266-18T 2020-01-10 08800017262970 EXULT Knee Replacement System K3.IBN.4469-09T 2020-01-10 08800017262987 EXULT Knee Replacement System K3.IBN.4469-10T 2020-01-10 08800017262994 EXULT Knee Replacement System K3.IBN.4469-11T 2020-01-10 08800017263007 EXULT Knee Replacement System K3.IBN.4469-12T 2020-01-10 08800017263014 EXULT Knee Replacement System K3.IBN.4469-13T 2020-01-10 08800017263021 EXULT Knee Replacement System K3.IBN.4469-14T 2020-01-10 08800017263038 EXULT Knee Replacement System K3.IBN.4469-16T 2020-01-10 08800017263045 EXULT Knee Replacement System K3.IBN.4469-18T 2020-01-10 08800017263052 EXULT Knee Replacement System K3.IBN.4572-09T 2020-01-10 08800017263069 EXULT Knee Replacement System K3.IBN.4572-10T 2020-01-10 08800017263076 EXULT Knee Replacement System K3.IBN.4572-11T 2020-01-10 08800017263083 EXULT Knee Replacement System K3.IBN.4572-12T 2020-01-10 08800017263090 EXULT Knee Replacement System K3.IBN.4572-13T 2020-01-10 08800017263106 EXULT Knee Replacement System K3.IBN.4572-14T 2020-01-10 08800017263113 EXULT Knee Replacement System K3.IBN.4572-16T 2020-01-10
Other Devices Sharing Product Codes# 
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