Home GUDID 00887868071065 1/3 COMPOSITE RING, MEDIUM
Primary DI 00887868071065
Brand 1/3 COMPOSITE RING, MEDIUM
Company Biomet Orthopedics, LLC
Model FC-10030
Catalog number FC10030
Published 2015-10-24
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true
Product Codes# Code, Name table Code Name JDW PIN, FIXATION, THREADED KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT LXT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class JDW Pin, Fixation, Threaded Orthopedic 2 KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic 2 LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00887868071065 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 00887868071065 00887868071065 887868071065 0887868071065
GMDN Terms# Term, Definition table Term Definition External orthopaedic fixation system, single-use, non-sterile An assembly of non-sterile devices designed to stabilize fractured bones to promote treatment and healing. It typically consists of an external plastic and/or metallic fixator (a framework) and other external and/or implantable components such as clamps, rods, rings, pins, bolts, and nuts, as well as some reusable instrumentation (e.g., wrenches, depth gauge, tensioner). It is used mainly to help the healing of long bones such as the femur, tibia and humerus, as well as fractures of the foot and ankle, joint fusions, and limb lengthening. This is a single-use device intended to be sterilized prior to use.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 129278169 Device count 1 Lot or batch true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00880304474185 Arcos® Modular Revision Hip System 11-302102 11-302102 2015-10-24 00880304474246 Arcos® Modular Revision Hip System 11-302101 11-302101 2015-10-24 00880304539259 Arcos® Modular Revision Hip System 11-302109 11-302109 2015-10-24 00889024711280 Jgrknt Reusable Fishmouth Perc Guide SSI008662 SSI008662 2026-08-25 00889024712034 Percutaneous Soft Anchor Short 1.4mm Guide SSI008661 SSI008661 2026-08-25 00880304527386 Active Articulation 010000990 010000990 2020-05-15 00880304527393 Active Articulation 010000991 010000991 2020-05-15 00880304485020 Active Articulation Hip System EP-200144 EP-200144 2015-11-03 00880304485037 Active Articulation Hip System EP-200146 EP-200146 2015-11-03 00880304485044 Active Articulation Hip System EP-200148 EP-200148 2015-10-24 00880304485051 Active Articulation Hip System EP-200150 EP-200150 2015-10-24 00880304485068 Active Articulation Hip System EP-200152 EP-200152 2015-10-24 00880304485075 Active Articulation Hip System EP-200154 EP-200154 2015-10-24 00880304485082 Active Articulation Hip System EP-200156 EP-200156 2015-10-24 00880304485099 Active Articulation Hip System EP-200158 EP-200158 2015-10-24 00880304485105 Active Articulation Hip System EP-200160 EP-200160 2015-10-24 00880304485112 Active Articulation Hip System EP-200162 EP-200162 2015-10-24 00880304485129 Active Articulation Hip System EP-200164 EP-200164 2015-11-04 00880304485136 Active Articulation Hip System EP-200166 EP-200166 2015-10-24 00880304491328 Active Articulation™ Dual Mobility Hip System XL-200144 XL-200144 2015-10-24
Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 07613327616859 HOFFMANN LRF Stryker GmbH KTT 2026-07-23 07613327616880 HOFFMANN LRF Stryker GmbH KTT 2026-07-23 18032568033229 Surgical Instruments ORTHOFIX SRL JDW 2026-07-23 18032568033236 Surgical Instruments ORTHOFIX SRL JDW 2026-07-23 18032568036008 WRIST FIXATION SYSTEMS ORTHOFIX SRL JDW 2026-07-23 07613327616835 HOFFMANN LRF Stryker GmbH KTT 2026-07-21 07613327616866 HOFFMANN LRF Stryker GmbH KTT 2026-07-21 07613327618501 HOFFMANN LRF Stryker GmbH JDW 2026-07-21 10888867544571 Arthrex® ARTHREX, INC. KTT 2026-03-13 00887868549236 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549243 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549250 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549267 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549274 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549281 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549298 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549304 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549311 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549328 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549335 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549342 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549359 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549366 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549373 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868549380 MULTI-DIRECTIONAL SCREW Biomet Orthopedics, LLC LXT 2022-11-14 00887868544699 SMOOTH PEG Biomet Orthopedics, LLC LXT 2022-09-07 00887868544705 SMOOTH PEG Biomet Orthopedics, LLC LXT 2022-09-07 00887868544712 SMOOTH PEG Biomet Orthopedics, LLC LXT 2022-09-07 00887868544729 SMOOTH PEG Biomet Orthopedics, LLC LXT 2022-09-07 00887868544736 SMOOTH PEG Biomet Orthopedics, LLC LXT 2022-09-07