ULTRAFIX 10121

GUDID 20845854024192

ULTRAFIX ARTHROSCOPIC INSERTER

Conmed Corporation

Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver

• Primary Device ID: 20845854024192
• NIH Device Record Key: ac0c33f0-72f8-49d3-8182-9b1919ad3af0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ULTRAFIX
• Version Model Number: 10121
• Catalog Number: 10121
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10845854024195 [Primary]
GS1	20845854024192 [Direct Marking]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

[20845854024192]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-09-28
• Device Publish Date: 2020-09-24

On-Brand Devices [ULTRAFIX]

• 30845854037144: ULTRAFIX MICROMITE DRILL, 1.8MM
• 30845854037113: ULTRAFIX ARTHROSCOPIC DRILL, 2.4MM
• 30845854037106: ULTRAFIX DRILL, 2.4MM
• 30845854037076: ULTRAFIX ARTHROSCOPIC DRILL GUIDE
• 30845854037021: ULTRAFIX DRILL 3.2MM
• 30845854037014: ULTRAFIX DRILL GUIDE
• 30845854024199: ULTRAFIX ARTHROSCOPIC INSERTER
• 20845854024192: ULTRAFIX ARTHROSCOPIC INSERTER
• 20845854037062: ULTRAFIX ARTHROSCOPIC DRILL, 3.2MM
• 20845854037024: ULTRAFIX DRILL 3.2MM