Home GUDID 00841732151239
PREFERENCE Pedicle Screw System
Primary DI 00841732151239
Brand PREFERENCE Pedicle Screw System
Company CTL Medical Corporation
Model 25-8000-018
Device description Lateral Offset 18mm
Published 2024-11-01
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Single use true
Product Codes# Code, Name table Code Name KWP Appliance, Fixation, Spinal Interlaminal KWQ Appliance, Fixation, Spinal Intervertebral Body MNI Orthosis, Spinal Pedicle Fixation
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 MNI Orthosis, Spinal Pedicle Fixation Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00841732151239 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00841732151239 00841732151239 841732151239 0841732151239
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system connector An implantable, small connecting component of a bone-screw internal spinal fixation system typically in the form of a thin band or small rod with a groove or hole at one or both ends, into which the screw heads and/or primary rods fit, intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, and also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. It is designed as a transverse or longitudinal connecting element to be attached to the corresponding screw heads and/or primary rods; it may also have adjustable length and/or angle and/or allow a small amount of screw/rod movement.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 080138504 Device count 1 Lot or batch true Manufacturing date on label 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 04052536163403 neon3 Ulrich GmbH & Co. KG KWP 2026-06-09 04052536163410 neon3 Ulrich GmbH & Co. KG KWP 2026-06-09 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