Reprocessed Large Tear Cross Cut Rasp, 14.0mm x 7.0mm

GUDID B3905100371141

SURETEK MEDICAL

Burring power tool attachment

• Primary Device ID: B3905100371141
• NIH Device Record Key: bf7e56de-dae4-41f6-a3a3-98ecc3a9cbb7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed Large Tear Cross Cut Rasp, 14.0mm x 7.0mm
• Version Model Number: 5100-37-114
• Company DUNS: 785616934
• Company Name: SURETEK MEDICAL
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B3905100371141 [Primary]

FDA Product Code

• HTR: Rasp

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: 2024-02-20
• Device Publish Date: 2024-02-12

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