Reprocessed Micro Oscillating Sagittal Blade,18 x 5.5 mm

GUDID B390229632121

SURETEK MEDICAL

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• Primary Device ID: B390229632121
• NIH Device Record Key: f7609f38-51e0-491a-be4d-b556260fd5c9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed Micro Oscillating Sagittal Blade,18 x 5.5 mm
• Version Model Number: 2296-3-212
• 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	B390229632121 [Primary]

FDA Product Code

• GFA: Blade, Saw, General & Plastic Surgery, Surgical

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: 2021-05-04
• Device Publish Date: 2021-04-26

On-Brand Devices [Reprocessed Micro Oscillating Sagittal Blade,18 x 5.5 mm]

• B3902296332121: 2296-33-212
• B390229632121: 2296-3-212