Home GUDID 00846468004088 RELEASE LAMINOPLASTY FIXATION SYSTEM
Primary DI 00846468004088
Brand RELEASE LAMINOPLASTY FIXATION SYSTEM
Company Pioneer Surgical Technology, Inc.
Model 725-081
Catalog number 725-081
Device description LAMINOPLASTY, Ø1.2mm x 4mm DRILL ASSY
Published 2019-06-13
Public version status Update
Distribution status Not in Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true Product Codes# Code, Name table Code Name LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT NQW ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class LXH Orthopedic Manual Surgical Instrument Orthopedic 1 NQW Orthosis, Spine, Plate, Laminoplasty, Metal Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00846468004088 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 00846468004088 00846468004088 846468004088 0846468004088
GMDN Terms# Term, Definition table Term Definition Orthopaedic prosthesis implantation instrument, reusable A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments. It may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components. This is a reusable device intended to be sterilized prior to use.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 793384496 Device count 1 Premarket exempt true Lot or batch true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00840298703685 CODA™ Anterior Cervical Plate System 58-202230010S 2022-30-010S 2023-06-28 00840298703708 CODA™ Anterior Cervical Plate System 58-202230014S 2022-30-014S 2023-06-28 00840298701445 CODA™ Anterior Cervical Plate System 58-102201010S 1022-01-010S 2023-06-26 00840298701452 CODA™ Anterior Cervical Plate System 58-102201012S 1022-01-012S 2023-06-26 00840298701469 CODA™ Anterior Cervical Plate System 58-102201014S 1022-01-014S 2023-06-26 00840298701476 CODA™ Anterior Cervical Plate System 58-102201016S 1022-01-016S 2023-06-26 00840298701490 CODA™ Anterior Cervical Plate System 58-102201020S 1022-01-020S 2023-06-26 00840298701506 CODA™ Anterior Cervical Plate System 58-102201022S 1022-01-022S 2023-06-26 00840298701520 CODA™ Anterior Cervical Plate System 58-102201026S 1022-01-026S 2023-06-26 00840298701537 CODA™ Anterior Cervical Plate System 58-102201028S 1022-01-028S 2023-06-26 00840298701544 CODA™ Anterior Cervical Plate System 58-102201030S 1022-01-030S 2023-06-26 00840298701568 CODA™ Anterior Cervical Plate System 58-102202026S 1022-02-026S 2023-06-26 00840298701582 CODA™ Anterior Cervical Plate System 58-102202030S 1022-02-030S 2023-06-26 00840298701599 CODA™ Anterior Cervical Plate System 58-102202032S 1022-02-032S 2023-06-26 00840298701605 CODA™ Anterior Cervical Plate System 58-102202034S 1022-02-034S 2023-06-26 00840298701612 CODA™ Anterior Cervical Plate System 58-102202036S 1022-02-036S 2023-06-26 00840298701629 CODA™ Anterior Cervical Plate System 58-102202038S 1022-02-038S 2023-06-26 00840298701636 CODA™ Anterior Cervical Plate System 58-102202040S 1022-02-040S 2023-06-26 00840298701643 CODA™ Anterior Cervical Plate System 58-102202042S 1022-02-042S 2023-06-26 00840298701650 CODA™ Anterior Cervical Plate System 58-102202044S 1022-02-044S 2023-06-26
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