DUAFIT A60 SP106

GUDID 03760225718735

DUAFIT PIP 10° PEEK STERILE SIZE 2L

IN2BONES

Interphalangeal joint arthrodesis implant

• Primary Device ID: 03760225718735
• NIH Device Record Key: a3f067ca-08f0-46e6-a210-c08367f283a3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DUAFIT
• Version Model Number: A60 SP106
• Catalog Number: A60 SP106
• Company DUNS: 263616749
• Company Name: IN2BONES
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03760225718735 [Primary]

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-12-23
• Device Publish Date: 2024-12-13

On-Brand Devices [DUAFIT]

• 03760225712993: A06 10401
• 03760225718759: DUAFIT PIP 17° PEEK STERILE SIZE 2L
• 03760225718742: DUAFIT PIP 17° PEEK STERILE SIZE 1L
• 03760225718735: DUAFIT PIP 10° PEEK STERILE SIZE 2L
• 03760225718728: DUAFIT PIP 10° PEEK STERILE SIZE 1L
• 03701337603052: DUAFIT PIP 0° PEEK STERILE SIZE 2L
• 03701337603045: DUAFIT PIP 0° PEEK STERILE SIZE 1L