Home GUDID H981046074590 USS
Primary DI H981046074590
Brand USS
Company Synthes GmbH
Model 04.607.459
Catalog number 04607459
Device description 9.0MM TI USS CANC POLYAXIAL SCREW 65MM THREAD LENGTH
Published 2015-09-14
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use true Product Codes# Code, Name table Code Name KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10705034736747 Primary GS1 0 H981046074590 Secondary HIBCC 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10705034736747 10705034736747
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system, non-sterile An assembly of non-sterile 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. Non-sterile disposable devices associated with implantation may be included.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 486711679 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false 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# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00193982239862 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982239886 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982239909 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982239923 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982239947 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982239961 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982240240 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982240363 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982240622 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982450151 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982450168 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982450175 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982450182 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982450199 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521134 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521141 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521158 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521165 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521172 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521189 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521196 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521202 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521219 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521226 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521233 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521240 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521257 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521264 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521271 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982669638 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14
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