Home GUDID 00888867217577 Arthrex®
Primary DI 00888867217577
Brand Arthrex®
Company ARTHREX, INC.
Model AR-5051-32
Catalog number AR-5051-32
Device description LO-PRO SCRW, CANN, BLUNT TIP, 4 X 32 MM
Published 2017-02-15
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 HTY PIN, FIXATION, SMOOTH
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HTY Pin, Fixation, Smooth Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00888867217577 Primary GS1 0 M150AR5051320 Secondary HIBCC 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00888867217577 00888867217577 888867217577 0888867217577
GMDN Terms# Term, Definition table Term Definition Orthopaedic bone screw, non-bioabsorbable, non-sterile A small, non-sterile, threaded rod with a slotted head typically used for internal orthopaedic fracture fixation by being screwed into bone to hold plates or nails to bone or to provide direct interfragmentary stabilization of bone, or it may fasten soft tissue to bone; it is made of a material that cannot be chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). Screws available are: cortical, cancellous, malleolar, scaphoid, partially-threaded and fully-threaded, self-tapping, and cannulated. A "lag screw" can be any of these used to obtain compression. This device must be sterilized prior to use.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
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 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 24053613265496 Steinmann Pin Gebr. Brasseler GmbH & Co. KG HTY 2026-03-20 00888867516533 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867516564 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867516601 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543188 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543270 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543287 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543294 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543317 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543324 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543485 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543621 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543652 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543669 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543683 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543812 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543829 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543850 Arthrex® ARTHREX, INC. HTY 2026-03-13 00888867543874 Arthrex® ARTHREX, INC. HTY 2026-03-13 24026704912432 KMEDIC TELEFLEX INCORPORATED HTY 2026-02-06 06438394000018 ActivaPin™ Bioretec Oy HTY 2026-02-05 06438394000025 ActivaPin™ Bioretec Oy HTY 2026-02-05 06438394000032 ActivaPin™ Bioretec Oy HTY 2026-02-05 06438394000049 ActivaPin™ Bioretec Oy HTY 2026-02-05 06438394000056 ActivaPin™ Bioretec Oy HTY 2026-02-05 06438394000063 ActivaPin™ Bioretec Oy HTY 2026-02-05 06438394000070 ActivaPin™ Bioretec Oy HTY 2026-02-05 06438394000087 ActivaPin™ Bioretec Oy HTY 2026-02-05 06438394000094 ActivaPin™ Bioretec Oy HTY 2026-02-05 06438394000100 ActivaPin™ Bioretec Oy HTY 2026-02-05
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