REVO C6102B

GUDID 10845854026717

Thin Shaft Revo Driver

Conmed Corporation

Orthopaedic implant driver

• Primary Device ID: 10845854026717
• NIH Device Record Key: b9976eed-f6e8-4cac-ba31-9a7aedd185e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REVO
• Version Model Number: C6102B
• Catalog Number: C6102B
• 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(800)237-0169
• Email: CUSTOMER_SERVICE@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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10845854026717 [Primary]
GS1	20845854026714 [Direct Marking]

FDA Product Code

• GFG: BIT, SURGICAL

Sterilization

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

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

[10845854026717]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-05-06
• Device Publish Date: 2020-04-28

On-Brand Devices [REVO]

• 20845854019792: 4MM REVO ANCHOR, PRETHREADED, TWO No. 2 (5 METRIC) HI-FI
• 20845854019785: 4MM REVO ANCHOR, PRETHREADED, No. 2 (5 METRIC) HI-FI
• 10845854026717: Thin Shaft Revo Driver
• 20845854030759: MINI-REVO DRILL, 1.5MM
• 20845854030834: MINI-REVO TAP
• 20845854030742: MINI-REVO BONE PUNCH 1.5MM
• 20845854030728: MINI-REVO DRIVER
• 20845854030704: 2MM REVO BONE PUNCH
• 20845854030674: REVO CROCHET HOOK
• 30845854030763: MINI-REVO DRILL GUIDE, 1.5MM
• 10845854015070: REVO SCREW PRELOADED