Home GUDID H679040130430 EXPert Nail
Primary DI H679040130430
Brand EXPert Nail
Company Synthes GmbH
Model 04.013.043
Catalog number 04013043
Device description TI SPIRAL BLADE 55MM FOR TI RETROGRADE FEMORAL NAILS-EX
Published 2015-09-14
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 HWC Screw, fixation, bone
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HWC Screw, Fixation, Bone Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10886982087409 Primary GS1 0 H679040130430 Secondary HIBCC 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10886982087409 10886982087409
GMDN Terms# Term, Definition table Term Definition Spiral blade An implantable, rod-like, cannulated device with spiralled flutes at the distal end and a smooth cylindrical portion at the proximal end that is used in combination with a bone fixation plate or an intramedullary nail to support bone fragments after fractures, particularly in the proximal femur or proximal humerus (the bone heads). It is made of metal that cannot be chemically degraded (e.g., surgical steel, titanium alloy). It is intended to decrease the amount of removed bone required for device insertion, and provides a support surface in the zone requiring support (bone head) and resistance to bending in the zone most subject to torque.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 486711679 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 05055662970890 ORTHO SOLUTIONS SUCCESSION AFN SYSTEM ORTHO SOLUTIONS HOLDINGS LIMITED HWC 2026-07-10 05055662971514 ORTHO SOLUTIONS SUCCESSION AFN SYSTEM ORTHO SOLUTIONS HOLDINGS LIMITED HWC 2026-07-10 00885556904879 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556904923 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906163 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906170 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906187 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906194 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906200 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906217 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906224 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906231 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906248 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906255 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906262 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906279 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906286 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906293 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906309 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906316 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556906323 EVOS Smith & Nephew, Inc. HWC 2026-06-25 00885556901946 EVOS Smith & Nephew, Inc. HWC 2026-06-24 00888867460973 Arthrex® ARTHREX, INC. HWC 2026-06-11 00193982586393 CAPTIVATE GLOBUS MEDICAL, INC. HWC 2026-06-10 00193982586416 CAPTIVATE GLOBUS MEDICAL, INC. HWC 2026-06-10 00193982586430 CAPTIVATE GLOBUS MEDICAL, INC. HWC 2026-06-10 00193982586454 CAPTIVATE GLOBUS MEDICAL, INC. HWC 2026-06-10 00193982586478 CAPTIVATE GLOBUS MEDICAL, INC. HWC 2026-06-10 00193982586690 CAPTIVATE GLOBUS MEDICAL, INC. HWC 2026-06-10 00193982586706 CAPTIVATE GLOBUS MEDICAL, INC. HWC 2026-06-10
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