Home GUDID 00852776006614 CORUS PCSS 3D LevelOne, 4mm
Primary DI 00852776006614
Brand CORUS PCSS 3D LevelOne, 4mm
Company Providence Medical Technology, Inc.
Model DX-50-413
Device description The CORUS Spinal System-X is a set of instruments indicated to be used to perform posterior cervical fusion in patients with cervical degenerative disc disease. CORUS Posterior Cervical Stabilization System 3D (CORUS PCSS 3D) is posterior spinal instrumentation with integrated screw fixation intended to provide immobilization and stabilization of spinal segments. DiViNE Portal System is a set of instruments indicated to make the interior of a joint visible and/or to perform surgery within a joint.
Published 2026-09-30
Public version status New
Distribution status In Commercial Distribution
MRI safety MR Conditional
Rx true
OTC false
Sterile true
Single use true
Product Codes# Code, Name table Code Name MRW System, Facet Screw Spinal Device
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MRW System, Facet Screw Spinal Device Unknown U
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00852776006614 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 00852776006614 00852776006614 852776006614 0852776006614
GMDN Terms# Term, Definition table Term Definition Internal spinal fixation procedure kit, single-use A collection of various orthopaedic manual surgical instruments (e.g., screwdriver, trial rod, adaptor, mallet, guide tube, chisel, rasp, awl, burr, tap, drill) intended to be used to perform a bone-screw internal spinal fixation and/or spinal fusion cage implantation procedure (including stereotactic procedures); implanted devices are not included. This is a single-use device.
Regulatory Flags# DUNS number 969820245 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 true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00888867614543 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614550 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614567 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614574 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614581 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614598 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614604 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614611 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614628 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614635 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614642 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614659 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614666 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614673 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614680 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614697 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614703 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614710 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614727 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614734 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614741 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614758 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614765 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614772 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614789 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614796 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614802 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614819 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614826 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614833 Arthrex® ARTHREX, INC. MRW 2026-10-07