Rasp

GUDID 00810111225144

Rasp

Treace Medical Concepts, Inc.

Bone file/rasp, manual, reusable

• Primary Device ID: 00810111225144
• NIH Device Record Key: 0acdeeb8-6914-4890-a7f4-d6d4e614ace4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rasp
• Version Model Number: 02-00420
• Company DUNS: 054808082
• Company Name: Treace Medical Concepts, Inc.
• 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	00810111225144 [Primary]

FDA Product Code

• HTR: Rasp

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-10-01
• Device Publish Date: 2025-09-23

On-Brand Devices [Rasp]

• 00810111224284: MIS Rasp
• 00810111225144: Rasp