Home GUDID 23596010083078 NA
Primary DI 23596010083078
Brand NA
Company Smith & Nephew, Inc.
Model 128130
Catalog number 128130
Device description STEINMANN PIN DIAMOND POINT ROUND END 5/32 X 9
Published 2015-08-29
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 23596010083078 Package GS1 6 In Commercial Distribution 03596010083074 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 23596010083078 23596010083078 03596010083074 03596010083074 3596010083074
GMDN Terms# Term, Definition table Term Definition Orthopaedic bone pin, non-bioabsorbable A small diameter rod typically used for the fixation of a bone fracture or bone grafts, or for an osteotomy or arthrodesis. The rod may be smooth, wholly- or partially-threaded, solid or cannulated, and some designs may be tapered; it is not specific to the clavicle bone. The device is made of a material that is not chemically degraded or absorbed by natural body processes (e.g., implant grade metal, surgical steel, titanium alloy, or carbon fibre). Some designs may have a break-off shank and/or may be coated [e.g., with hydroxyapatite, also known as hydroxylapatite (HA)] to improve purchase in osteoporotic bone and for long-term fixation. This is a single-use device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 109903521 Device count 1 DM exempt false Premarket exempt true 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