DUAFIT

GUDID 03760225712993

IN2BONES

Orthopaedic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 03760225712993
• NIH Device Record Key: 59ea9985-ef24-444b-bf7a-f980934c4bf8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DUAFIT
• Version Model Number: A06 10401
• Company DUNS: 263616749
• Company Name: IN2BONES
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03760225712993 [Primary]

FDA Product Code

• KDD: Kit, Surgical Instrument, Disposable

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-12-09
• Device Publish Date: 2020-06-11

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