Reprocessed 2.9mm Serrated Blade, Rotatable

GUDID B39018829021

Reprocessed 2.9mm Serrated Blade, Rotatable, without Tubing

SURETEK MEDICAL

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• Primary Device ID: B39018829021
• NIH Device Record Key: 25942db5-4e5e-4c51-8982-f340a30a97f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed 2.9mm Serrated Blade, Rotatable
• Version Model Number: 18-82902HR
• 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	B39018829021 [Primary]

FDA Product Code

• NBH: Accessories, Arthroscopic

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: 2019-05-14
• Device Publish Date: 2019-05-06

On-Brand Devices [Reprocessed 2.9mm Serrated Blade, Rotatable]

• B39018829021: Reprocessed 2.9mm Serrated Blade, Rotatable, without Tubing
• B3901882902HR1: 18-82902HR