Home GUDID 00845694002424 OsteoMed
Primary DI 00845694002424
Brand OsteoMed
Company OSTEOMED LLC
Model 211-2005
Catalog number 211-2005
Device description 2.0mm x 5mm AUTO-DRIVE Screw
Published 2015-04-01
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 00845694002424 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 00845694002424 00845694002424 845694002424 0845694002424
GMDN Terms# Term, Definition table Term Definition Craniofacial bone screw, non-bioabsorbable, sterile A small, sterile, threaded rod with a slotted head intended to be implanted or inserted short-term in craniofacial bone (including the maxilla and/or mandible) for fracture fixation by direct interfragmentary stabilization of bone or by screwing plates in place; it may also be intended for transplanted bone fixation. It may be self-drilling/self-tapping and is made of a material that is not chemically degraded or absorbed via natural body processes [e.g., implant grade metal such as titanium (Ti)]. Its uses include repair of orbital fractures and fractures around the cranial sinuses, paediatric reconstructive surgery, craniotomy flap fixation, bone augmentation procedures.
Device Sizes# Type, Value, Unit table Type Value Unit Length 5 Millimeter
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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