Home GUDID 20887587042791
PlusDrive
Primary DI 20887587042791
Brand PlusDrive
Company Synthes GmbH
Model 400.412
Catalog number 400412
Device description 1.0MM TI CRTX SCREW SLF-TPNG W/PLUSDRIVE(TM) RECESS 12MM
Published 2015-09-14
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true
Product Codes# Code, Name table Code Name DZL SCREW, FIXATION, INTRAOSSEOUS HWC Screw, fixation, bone MQN EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DZL Screw, Fixation, Intraosseous Dental 2 HWC Screw, Fixation, Bone Orthopedic 2 MQN External Mandibular Fixator And/Or Distractor Dental 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 20887587042791 Primary GS1 0 H9804004120 Secondary HIBCC 0 80887587042793 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 20887587042791 20887587042791 80887587042793 80887587042793
GMDN Terms# Term, Definition table 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.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 486711679 Device count 5 Lot or batch true 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 03700569658212 Xpert PFP NEWCLIP TECHNICS HWC 2026-06-03 00842188131981 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188131998 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132001 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132018 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132025 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132032 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132049 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132056 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132063 Tools - HCS Trimed, INC. HWC 2026-06-02 00842188132070 Tools - HCS Trimed, INC. HWC 2026-06-02 07630894829819 APTUS Medartis AG HWC 2026-06-01 07630894829826 APTUS Medartis AG HWC 2026-06-01 07630894829833 APTUS Medartis AG HWC 2026-06-01 07630894829840 APTUS Medartis AG HWC 2026-06-01 07630894829857 APTUS Medartis AG HWC 2026-06-01 07630894829864 APTUS Medartis AG HWC 2026-06-01 07630894829871 APTUS Medartis AG HWC 2026-06-01 07630894829888 APTUS Medartis AG HWC 2026-06-01 07630894829895 APTUS Medartis AG HWC 2026-06-01 07630894829901 APTUS Medartis AG HWC 2026-06-01 07630894829918 APTUS Medartis AG HWC 2026-06-01 07630894829925 APTUS Medartis AG HWC 2026-06-01 07630894829932 APTUS Medartis AG HWC 2026-06-01 07630894829949 APTUS Medartis AG HWC 2026-06-01 07630894829956 APTUS Medartis AG HWC 2026-06-01 07630894829963 APTUS Medartis AG HWC 2026-06-01 07630894829970 APTUS Medartis AG HWC 2026-06-01 07630894829987 APTUS Medartis AG HWC 2026-06-01 07630894829994 APTUS Medartis AG HWC 2026-06-01