Home GUDID 00845694036566 OsteoMed
Primary DI 00845694036566
Brand OsteoMed
Company OSTEOMED LLC
Model 320-1062
Catalog number 320-1062
Device description HPS 1.6mm Screw & Plate Module II
Published 2016-10-03
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 false 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 00845694036566 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 00845694036566 00845694036566 845694036566 0845694036566
GMDN Terms# Term, Definition table Term Definition General internal orthopaedic fixation system implantation kit A collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device.
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 Store at controlled room temperature, away from moisture and direct sunlight.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
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 true 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 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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