Reprocessed Arthrex 4.5mm Drill, Cannulated

GUDID B390AR1218451

Arthrex Drill, 4.5mm Cannulated

SURETEK MEDICAL

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• Primary Device ID: B390AR1218451
• NIH Device Record Key: 044b7cf0-ae85-4e27-86c1-c0f8d7671b49
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed Arthrex 4.5mm Drill, Cannulated
• Version Model Number: AR-1218-45
• 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	B390AR1218451 [Primary]

FDA Product Code

• HTW: Bit, Drill

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: 2023-03-27
• Device Publish Date: 2023-03-17

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