Home GUDID 00846468039318
Cross-Fuse PEEK IBF System
Primary DI 00846468039318
Brand Cross-Fuse PEEK IBF System
Company Pioneer Surgical Technology, Inc.
Model 35-DTRL18-9-6
Catalog number 35-DTRL18-9-6
Device description TRIAL SPACER
Published 2020-09-25
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 HWT TEMPLATE LXH Orthopedic manual surgical instrument
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HWT Template Orthopedic 1 LXH Orthopedic Manual Surgical Instrument Orthopedic 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00846468038694 Previous GS1 0 00191083032450 Primary GS1 0 00846468039318 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 00846468038694 00846468038694 846468038694 0846468038694 00191083032450 00191083032450 191083032450 0191083032450 00846468039318 00846468039318 846468039318 0846468039318
GMDN Terms# Term, Definition table Term Definition Surgical implant template, reusable A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device.
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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