Home GUDID 00846468061845 Cross-Fuse® PEEK VBR/IBF System
Primary DI 00846468061845
Brand Cross-Fuse® PEEK VBR/IBF System
Company Pioneer Surgical Technology, Inc.
Model 35-INSERTER2-14-CL
Catalog number 35-INSERTER2-14-CL
Device description INSERTER, MODULAR CLEANING
Published 2018-10-06
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 table Code Name HXX SCREWDRIVER
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HXX Screwdriver Orthopedic 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00846468061845 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 00846468061845 00846468061845 846468061845 0846468061845
GMDN Terms# Term, Definition table Term Definition Orthopaedic implant inserter/extractor, reusable A hand-held manual surgical instrument designed to insert or extract an implantable orthopaedic device (e.g., a bone nail, spiral blade, or bone fixation plate) through application of a striking or screwing force. It is an instrument in a one-piece or modular configuration with a mechanism that will attach and/or lock to part of the implant, and a mechanism to apply the striking force (e.g., on a pad/flange) using a surgical hammer or a weight that can slide along a shaft, or a mechanism for twisting (screwing) (e.g., T-handle). This is a reusable device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 793384496 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false 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# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00840298701902 CODA™ Anterior Cervical Plate System 58-202201010 2022-01-010 2023-01-19 00840298701971 CODA™ Anterior Cervical Plate System 58-202201024 2022-01-024 2023-01-19 00840298702039 CODA™ Anterior Cervical Plate System 58-202202028 2022-02-028 2023-01-19 00840298702268 CODA™ Anterior Cervical Plate System 58-202204080 2022-04-080 2023-01-19 00840298700134 CODA™ Anterior Cervical Plate System 58-202221018S 2022-21-018S 2023-01-19 00840298700028 CODA™ Anterior Cervical Plate System 58-202220014S 2022-20-014S 2023-01-19 00840298700110 CODA™ Anterior Cervical Plate System 58-202221014S 2022-21-014S 2023-01-19 00840298700677 CODA™ Anterior Cervical Plate System 58-202230200 2022-30-200 2023-01-24 00840298701957 CODA™ Anterior Cervical Plate System 58-202201020 2022-01-020 2023-01-19 00840298702022 CODA™ Anterior Cervical Plate System 58-202202026 2022-02-026 2023-01-19 00840298702251 CODA™ Anterior Cervical Plate System 58-202204076 2022-04-076 2023-01-19 00840298700608 CODA™ Anterior Cervical Plate System 58-202222200 2022-22-200 2023-01-24 00840298700776 CODA™ Anterior Cervical Plate System 58-202210007 2022-10-007 2023-01-25 00840298700905 CODA™ Anterior Cervical Plate System 58-202220717 2022-20-717 2023-01-19 00840298701933 CODA™ Anterior Cervical Plate System 58-202201016 2022-01-016 2023-01-19 00840298701988 CODA™ Anterior Cervical Plate System 58-202201026 2022-01-026 2023-01-19 00840298702091 CODA™ Anterior Cervical Plate System 58-202202040 2022-02-040 2023-01-19 00840298702114 CODA™ Anterior Cervical Plate System 58-202202044 2022-02-044 2023-01-19 00840298702138 CODA™ Anterior Cervical Plate System 58-202203045 2022-03-045 2023-01-19 00840298702176 CODA™ Anterior Cervical Plate System 58-202203057 2022-03-057 2023-01-19
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