Home GUDID 00842528103708 OsteoMed
Primary DI 00842528103708
Brand OsteoMed
Company OSTEOMED LLC
Model 319-0771
Catalog number 319-0771
Device description 7.0 x 70mm Cannulated Screw, 32mm Thd
Published 2017-09-22
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 HWC Screw, fixation, bone
Product Code Classifications Code Device Specialty Class HWC Screw, Fixation, Bone Orthopedic 2
Identifiers And Packaging Identifier Type Agency Package quantity Status 00842528103708 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier GTIN-14 normalized UPC-A EAN-13 00842528103708 00842528103708 842528103708 0842528103708
GMDN Terms Term Definition Orthopaedic bone screw, non-bioabsorbable, non-sterile A small, non-sterile, threaded rod with a slotted head typically used for internal orthopaedic fracture fixation by being screwed into bone to hold plates or nails to bone or to provide direct interfragmentary stabilization of bone, or it may fasten soft tissue to bone; it is made of a material that cannot be chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). Screws available are: cortical, cancellous, malleolar, scaphoid, partially-threaded and fully-threaded, self-tapping, and cannulated. A "lag screw" can be any of these used to obtain compression. This device must be sterilized prior to use.
Device Sizes Type Value Unit Length 70 Millimeter
Storage And Handling Type Low High Condition Special Storage Condition, Specify 0 0 Stored at controlled room temperature
Sterilization Methods 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 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