Reprocessed 3.5mm Tricut Blade

GUDID B39018835041

Reprocessed 3.5mm Tricut Blade, without Tubing

SURETEK MEDICAL

Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed Arthroscopic shaver system blade, reprocessed

• Primary Device ID: B39018835041
• NIH Device Record Key: db03e47f-a326-4b00-b100-49b41da48bf5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed 3.5mm Tricut Blade
• Version Model Number: 18-83504
• 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	B39018835041 [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 3.5mm Tricut Blade]

• B39018835041: Reprocessed 3.5mm Tricut Blade, without Tubing
• B3901883504T1: Reprocessed 3.5mm Tricut Blade, with Tubing