Home GUDID 00841132180761 Orthex Drill Cannulated
Primary DI 00841132180761
Brand Orthex Drill Cannulated
Company ORTHOPEDIATRICS CORP.
Model Z402-185-48
Catalog number Z402-185-48
Device description Drill, 2.0mm Solid, Short
Published 2020-03-02
Public version status New
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 GFG BIT, SURGICAL HTW Bit, Drill KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class GFG Bit, Surgical General, Plastic Surgery 1 HTW Bit, Drill Orthopedic 1 KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00841132180761 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 00841132180761 00841132180761 841132180761 0841132180761
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 796416191 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 00810168190457 NA PACIFIC INSTRUMENTS, INC. HTW 2026-05-26 04048844358617 MUTARS® implantcast GmbH HTW 2026-03-24 04048844358716 MUTARS® implantcast GmbH HTW 2026-03-24 04048844358792 MUTARS® implantcast GmbH HTW 2026-03-24 04048844358839 MUTARS® implantcast GmbH HTW 2026-03-24 00840314270245 gSource GSOURCE LLC HTW 2026-03-20 00840314270252 gSource GSOURCE LLC HTW 2026-03-20 00840314270269 gSource GSOURCE LLC HTW 2026-03-20 00763000884543 n/a MEDTRONIC SOFAMOR DANEK, INC. HTW 2026-03-13 00888867500891 Arthrex® ARTHREX, INC. HTW 2026-03-13 00888867500921 Arthrex® ARTHREX, INC. HTW 2026-03-13 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