Home GUDID 00886385015125 NA
Primary DI 00886385015125
Brand NA
Company Stryker Trauma SA
Model 451-1036
Catalog number 451-1036
Device description K-Wire, Single Trocar Point
Published 2015-09-24
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 00886385015125 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 00886385015125 00886385015125 886385015125 0886385015125
GMDN Terms# Term, Definition table Term Definition Orthopaedic bone wire A wire intended for the fixation of bone fractures that may be implanted or used short-term (e.g., to hold a plate in the correct position during an intervention). It may be used: 1) as a cerclage wire to aid bone fixation; 2) in a loop or figure-of-eight configuration to reattach, e.g., the tip of the elbow (olecranon), tibial tubercle, or greater trochanter; 3) to augment bone screw/plate fixation; or 4) as a Kirschner wire or K-Wire to stiffen (arthrodese) a toe or finger. It is made of metal [e.g., stainless steel, cobalt-chrome (Co-Cr)], and may be malleable or rigid; some types include a nut designed to be attached to the wire to prevent wire migration. This is a single-use device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Length 150 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 481999654 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