Home GUDID 04546540604675 NA
Primary DI 04546540604675
Brand NA
Company Stryker Trauma SA
Model 40-20909S
Catalog number 40-20909S
Device description DISTAL LATERAL FIBULA PLATE, 9 HOLE
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 true
Single use true Product Codes# Code, Name table Code Name KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 04546540604675 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 04546540604675 04546540604675 4546540604675
GMDN Terms# Term, Definition table Term Definition Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile A sterile assembly of implantable devices designed for the stabilization of fractured/surgically-cut bones of the limbs (long bones), their appendages (hands, feet), pelvis, craniomaxillofacial bones, and/or for limb-joint fusion. It typically consists of a set of bone fixation plates, screws, wires, and pins made of materials that cannot be chemically degraded or absorbed via natural body processes (e.g., implant grade metal, surgical steel, titanium alloy, or carbon fibre). It may also include instruments for the attachment of the implants such as screwdrivers or drills.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Length 149 Millimeter
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 true Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00888867516465 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867516472 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867518681 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543157 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543256 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543331 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543348 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543355 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543362 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543379 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543386 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543393 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543409 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543478 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543591 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543607 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543638 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543645 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543676 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543690 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543706 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543713 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543799 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543843 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543881 Arthrex® ARTHREX, INC. KTT 2026-03-13 00841731149077 DYNEX MICRO VILEX LLC KTT 2026-03-03 00889795151827 The Brachiator Mini External Fixation System Paragon 28, Inc. KTT 2025-12-16 00889795151834 The Brachiator Mini External Fixation System Paragon 28, Inc. KTT 2025-12-16 00889795151841 The Brachiator Mini External Fixation System Paragon 28, Inc. KTT 2025-12-16 00889795151858 The Brachiator Mini External Fixation System Paragon 28, Inc. KTT 2025-12-16