Reprocessed 2.9mm Serrated Blade, Rotatable

GUDID B3901882902HR1

SURETEK MEDICAL

Arthroscopic shaver system blade, reprocessed

• Primary Device ID: B3901882902HR1
• NIH Device Record Key: 4d57ba62-e39d-47fe-b48b-92cff564a6d6
• 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	B3901882902HR1 [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: 2022-03-21
• Device Publish Date: 2022-03-11

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

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