Home GUDID 00887868016172 CALIBRATED GUIDE WIRE, THREADED TROCAR POINT
Primary DI 00887868016172
Brand CALIBRATED GUIDE WIRE, THREADED TROCAR POINT
Company Biomet Orthopedics, LLC
Model 1601-20-000
Catalog number 160120000
Published 2016-10-14
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 00887868016172 Primary GS1 0 70887868016171 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00887868016172 00887868016172 887868016172 0887868016172 70887868016171 70887868016171
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.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 129278169 Device count 6 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
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