WEDGE BURR

GUDID 03760225713983

IN2BONES

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• Primary Device ID: 03760225713983
• NIH Device Record Key: 5d0ec94d-37be-4972-81bf-1b084ac098a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WEDGE BURR
• Version Model Number: G01 01452
• 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: 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	03760225713983 [Primary]

FDA Product Code

• GFF: Bur, Surgical, General & Plastic Surgery

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: 2020-06-17
• Device Publish Date: 2020-06-09

On-Brand Devices [WEDGE BURR]

• 03760225713983: G01 01452
• 03760225713884: G01 01451
• 03760225713945: G01 00972
• 03760225713938: G01 00962
• 03760225712481: G01 00971
• 03760225712474: G01 00961