Reprocessed Aggressive Medium Blade, 31 x 9 mm

GUDID B39022963525

SURETEK MEDICAL

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• Primary Device ID: B39022963525
• NIH Device Record Key: 47eba903-3a8b-45d1-a5ed-5027a73b931e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed Aggressive Medium Blade, 31 x 9 mm
• Version Model Number: 2296-3-525
• 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	B39022963525 [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: 2021-04-22
• Device Publish Date: 2021-04-14

On-Brand Devices [Reprocessed Aggressive Medium Blade, 31 x 9 mm]

• B39022963525: 2296-3-525
• B390229635251: 2296-3-525