Home GUDID 08806373842139 LOSPA IS Spinal System
Primary DI 08806373842139
Brand LOSPA IS Spinal System
Company Corentec Co., Ltd
Model SA.008.7535
Device description Polyaxial - Guided(Blasting)
Published 2015-10-21
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 08806373842139 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 08806373842139 08806373842139 8806373842139
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 08800017262178 EXULT Knee Replacement System K3.IAX.4469-09T 2020-01-10 08800017262185 EXULT Knee Replacement System K3.IAX.4469-10T 2020-01-10 08800017262192 EXULT Knee Replacement System K3.IAX.4469-11T 2020-01-10 08800017262208 EXULT Knee Replacement System K3.IAX.4469-12T 2020-01-10 08800017262215 EXULT Knee Replacement System K3.IAX.4469-13T 2020-01-10 08800017262222 EXULT Knee Replacement System K3.IAX.4469-14T 2020-01-10 08800017262239 EXULT Knee Replacement System K3.IAX.4469-16T 2020-01-10 08800017262246 EXULT Knee Replacement System K3.IAX.4469-18T 2020-01-10 08800017262253 EXULT Knee Replacement System K3.IAX.4572-09T 2020-01-10 08800017262260 EXULT Knee Replacement System K3.IAX.4572-10T 2020-01-10 08800017262277 EXULT Knee Replacement System K3.IAX.4572-11T 2020-01-10 08800017262284 EXULT Knee Replacement System K3.IAX.4572-12T 2020-01-10 08800017262291 EXULT Knee Replacement System K3.IAX.4572-13T 2020-01-10 08800017262307 EXULT Knee Replacement System K3.IAX.4572-14T 2020-01-10 08800017262314 EXULT Knee Replacement System K3.IAX.4572-16T 2020-01-10 08800017262321 EXULT Knee Replacement System K3.IAX.4572-18T 2020-01-10 08800017262338 EXULT Knee Replacement System K3.IAX.4775-09T 2020-01-10 08800017262345 EXULT Knee Replacement System K3.IAX.4775-10T 2020-01-10 08800017262352 EXULT Knee Replacement System K3.IAX.4775-11T 2020-01-10 08800017262369 EXULT Knee Replacement System K3.IAX.4775-12T 2020-01-10
Other Devices Sharing Product Codes# 
corentec.com