Home GUDID 00852776006300
ALLY™ Bone Screw-L 10mm
Primary DI 00852776006300
Brand ALLY™ Bone Screw-L 10mm
Company Providence Medical Technology, Inc.
Model PD-32-601
Catalog number PD-32-601
Device description The bone screw is indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation appropriate for the size of the device. Screws are intended for single use only.
Published 2016-09-27
Public version status Update
Distribution status In Commercial Distribution
MRI safety MR Unsafe
Rx true
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 10852776006307 Package GS1 1 In Commercial Distribution 00852776006300 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 10852776006307 10852776006307 00852776006300 00852776006300 852776006300 0852776006300
GMDN Terms# Term, Definition table Term Definition Spinal bone screw, non-bioabsorbable A small, threaded, implantable rod with a screw head and drive intended for internal spinal fixation by being screwed into the spine to hold a correction/stabilization device (e.g., rod, plate, tether) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (e.g., surgical steel, titanium alloy, carbon fibre). It is available in various types (e.g., pedicle or transfacet, with a slotted, cross, star, or polygonal drive), and is typically used to provide immobilization and stabilization of spinal segments in the treatment of spinal instabilities or deformities. A screw head adaptor intended to stabilize a rod may be included with the screw.
Sterilization Methods# Method table Method Radiation Sterilization
Regulatory Flags# DUNS number 969820245 Device count 1 DM exempt true Lot or batch true Manufacturing date on label true Expiration date on label 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