Home GUDID 00888867614567 Arthrex®
Primary DI 00888867614567
Brand Arthrex®
Company ARTHREX, INC.
Model AR-S8740-20HA-S
Catalog number AR-S8740-20HA-S
Device description Spine Compression Screw, 4.0x20mm, HA
Published 2026-10-07
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 HRC Sterilizer, soft-lens, thermal, battery-powered MRW SYSTEM, FACET SCREW SPINAL DEVICE
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HRC Sterilizer, Soft-Lens, Thermal, Battery-Powered Ophthalmic 2 MRW System, Facet Screw Spinal Device Unknown U
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00888867614567 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 00888867614567 00888867614567 888867614567 0888867614567
GMDN Terms# Term, Definition table Term Definition Spinal bone screw, non-bioabsorbable A small, threaded, implantable rod with a screw head and drive intended 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 (e.g., surgical steel, titanium alloy, carbon fibre). It is available in various types (e.g., pedicle or transfacet, with a slotted, cross, star, or polygonal drive), and is typically used to provide immobilization and stabilization of spinal segments in the treatment of spinal instabilities or deformities. A screw head adaptor intended to stabilize a rod may be included with the screw.
Regulatory Flags# DUNS number 131747628 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. HRC 2026-10-07 00888867614543 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614550 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614550 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614574 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614574 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614581 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614581 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614598 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614598 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614604 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614604 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614611 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614611 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614628 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614628 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614635 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614635 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614642 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614642 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614659 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614659 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614666 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614666 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614673 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614673 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614680 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614680 Arthrex® ARTHREX, INC. HRC 2026-10-07 00888867614697 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614697 Arthrex® ARTHREX, INC. HRC 2026-10-07
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