Argo Knotless GENESYS KBC4755RBP

GUDID 10653405988571

4.75/5.5 mm Argo KnotlessTM GENESYSTM Reusable Broaching Punch

Conmed Corporation

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• Primary Device ID: 10653405988571
• NIH Device Record Key: 8b032296-69f4-44df-bb71-f800185ac64f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Argo Knotless GENESYS
• Version Model Number: KBC4755RBP
• Catalog Number: KBC4755RBP
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY;DO NOT CRUSH

Device Identifiers

Device Issuing Agency	Device ID
GS1	10653405988571 [Direct Marking]
GS1	30653405988575 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

[10653405988571]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-22
• Device Publish Date: 2024-04-12

On-Brand Devices [Argo Knotless GENESYS]

• 10653405988601: 4.75 mm Argo KnotlessTM GENESYSTM Reusable Smooth Punch
• 10653405988595: 5.5 mm Argo KnotlessTM GENESYSTM Reusable Tap
• 10653405988588: 4.75 mm Argo KnotlessTM GENESYSTM Reusable Tap
• 10653405988571: 4.75/5.5 mm Argo KnotlessTM GENESYSTM Reusable Broaching Punch
• 30653405988766: 4.75/5.5 mm Argo KnotlessTM GENESYSTM Disposable Broaching Punch
• 30653405988759: 4.75 mm Argo KnotlessTM GENESYSTM Disposable Smooth Punch
• 30653405988742: 4.75 mm Argo KnotlessTM GENESYSTM Disposable Tap
• 30653405988735: 5.5 mm Argo KnotlessTM GENESYSTM Disposable Tap
• 30653405988698: 4.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, White/Black
• 30653405988681: 4.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, Blue/Blue
• 30653405988674: 4.75mm Argo Knotless® GENESYSTM Anchor
• 30653405988667: 5.5mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, White/Black
• 30653405988650: 5.5mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, Blue/Blue
• 30653405988643: 5.5mm Argo Knotless® GENESYSTM Anchor