Home GUDID 00845694068062 OsteoMed
Primary DI 00845694068062
Brand OsteoMed
Company OSTEOMED LLC
Model 316-0123-SP-05
Catalog number 316-0123-SP-05
Device description .045"x 4", K-wire, Double Trocar Sterile Qty 5
Published 2016-07-21
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 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 00845694068062 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 00845694068062 00845694068062 845694068062 0845694068062
GMDN Terms# Term, Definition table Term Definition Craniofacial fixation plate kit, non-bioabsorbable A collection of small sheets of firm material and bone screws, of various shapes/sizes, that are implanted onto fractured craniofacial bone (including the maxilla and/or mandible) to bridge and stabilize the fracture gap, and shield the site from stress as the bone heals; the components are made of a material that is not chemically degraded or absorbed by natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). Tools for implantation may be included. The device may also be used for craniofacial reconstructive procedures (e.g., to treat congenital malformations), endobrow fixation, or craniotomy flap fixation.
Device Sizes# Type, Value, Unit table Type Value Unit Outer Diameter 0.045 Inch
Storage And Handling# Type, Low, High table Type Low High Condition Handling Environment Temperature 0 275 Degrees Fahrenheit
Regulatory Flags# DUNS number 606417780 Device count 1 DM exempt true 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 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 00810211040227 Headed Screw Partially Threaded Short 3.0mm,30mm Length Pace Surgical, Inc. HWC 2026-03-19 08059386744369 RONDO' CITIEFFE SRL HWC 2026-03-17 00888867529038 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529083 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529090 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529113 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529144 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529151 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529182 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529212 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529373 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529434 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529441 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867529526 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867531918 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867531932 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867531949 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867531963 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867531970 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867531987 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867532007 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867532014 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867532069 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867532083 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867532137 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867532144 Arthrex® ARTHREX, INC. HWC 2026-03-16 00888867532281 Arthrex® ARTHREX, INC. HWC 2026-03-16 04053613298315 Guide Pin Smooth Gebr. Brasseler GmbH & Co. KG HWC 2026-03-11 00840124525474 PolyLock Midfoot FUSION ORTHOPEDICS, LLC HWC 2026-03-10 00840124525481 PolyLock Midfoot FUSION ORTHOPEDICS, LLC HWC 2026-03-10
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