Home GUDID 20845854655501 Argo Knotless
Primary DI 20845854655501
Brand Argo Knotless
Company Conmed Corporation
Model KBC475-KIT
Catalog number KBC475-KIT
Device description Argo Knotless Genesys Anchor Kit
Published 2026-09-25
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true
Product Codes# Code, Name table Code Name GAT Suture, nonabsorbable, synthetic, polyethylene LXH Orthopedic manual surgical instrument MAI Fastener, fixation, biodegradable, soft tissue MBI Fastener, fixation, nondegradable, soft tissue ORQ Mesh, surgical, deployer OWW Mesh, surgical, absorbable, orthopaedics, reinforcement of tendon OWY Mesh, surgical, collagen, orthopaedics, reinforcement of tendon
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery 2 LXH Orthopedic Manual Surgical Instrument Orthopedic 1 MAI Fastener, Fixation, Biodegradable, Soft Tissue Orthopedic 2 MBI Fastener, Fixation, Nondegradable, Soft Tissue Orthopedic 2 ORQ Mesh, Surgical, Deployer General, Plastic Surgery 2 OWW Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon General, Plastic Surgery 2 OWY Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon General, Plastic Surgery 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 30845854655508 Package GS1 1 In Commercial Distribution 20845854655501 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 30845854655508 30845854655508 20845854655501 20845854655501
GMDN Terms# Term, Definition table Term Definition Arthroscopic surgical procedure kit, non-medicated, single-use A collection of various sterile surgical and endoscopic instruments, dressings, and additional materials intended to be used specifically to perform an arthroscopic surgical procedure. It does not contain any pharmaceuticals. This is a single-use device.
Storage And Handling# Type, Low, High table Type Low High Condition Handling Environment Temperature 0 0 Special Storage Condition, Specify 0 0 KEEP DRY Storage Environment Temperature 0 0
Sterilization Methods# Method table Method Ethylene Oxide Radiation Sterilization
Regulatory Flags# DUNS number 071595540 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit true Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false 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 00824846013082 Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC. LXH 2026-10-19 00850078396440 SYNQ Single-Use Instrument System(1066) Eca Medical Instruments LXH 2026-10-19 00889024715295 Persona Extended V/V Guide Assembly (MFS) Zimmer, Inc. LXH 2026-10-19 08809986489807 LnK Spinal Instrument System L&K BIOMED CO. ,LTD. LXH 2026-10-19 00810111228671 Cut Guide Treace Medical Concepts, Inc. LXH 2026-10-16 00810129094503 InSet Subscap Repair Kit Threadstone LLC GAT 2026-10-16 00810161900305 EARP, TRIAL 22X35X12 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161900312 EARP, TRIAL 22X35X14 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161900329 EARP, TRIAL 22X35X12 12° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161900336 EARP, TRIAL 22X35X14 12° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901418 EARP TRIAL 22x40x10 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901425 EARP TRIAL 22x40x12 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901432 EARP TRIAL 22x40x14 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901449 EARP TRIAL 22x40x12 12° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901456 EARP TRIAL 22x40x14 12° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901463 EARP TRIAL 22x45x10 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901470 EARP TRIAL 22x45x12 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901487 EARP TRIAL 22x45x14 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901494 EARP TRIAL 22x45x12 12° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901500 EARP TRIAL 22x45x14 12° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901692 EARP TRIAL 22x50x10 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901708 EARP TRIAL 22x50x12 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901715 EARP TRIAL 22x50x14 6° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901722 EARP TRIAL 22x50x12 12° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00810161901739 EARP TRIAL 22x50x14 12° RETROPSOAS TECHNOLOGIES, LLC LXH 2026-10-16 00840606197007 MERCURY SPINAL ELEMENTS, INC. LXH 2026-10-16 00840606197014 MERCURY SPINAL ELEMENTS, INC. LXH 2026-10-16 00840606197021 MERCURY SPINAL ELEMENTS, INC. LXH 2026-10-16 00840606197038 MERCURY SPINAL ELEMENTS, INC. LXH 2026-10-16 05055662922622 Volition™ Plating System ORTHO SOLUTIONS HOLDINGS LIMITED LXH 2026-10-16