Home GUDID 07630030839801
M.U.S.T. Cross Connectors
Primary DI 07630030839801
Brand M.U.S.T. Cross Connectors
Company Medacta International SA
Model 03.56.064
Device description MUST LINK 64-98
Published 2014-09-17
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true Product Codes# Code, Name table Code Name KWP Appliance, Fixation, Spinal Interlaminal 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 KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2 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 07630030839801 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07630030839801 07630030839801 7630030839801
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system An assembly of 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. Disposable devices associated with implantation may be included.
Regulatory Flags# DUNS number 488227125 Device count 1 Lot or batch true Expiration date on label 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