Reprocessed 2.9mm Tricut Blade, Rotatable

GUDID B3901882094HR1

Reprocessed 2.9mm Tricut Blade, Rotatable, 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: B3901882094HR1
• NIH Device Record Key: 9b306564-341f-4e68-b080-c9ba6e835e35
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed 2.9mm Tricut Blade, Rotatable
• Version Model Number: 18-82904HR
• 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	B3901882094HR1 [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 Tricut Blade, Rotatable]

• B3901882094HR1: Reprocessed 2.9mm Tricut Blade, Rotatable, without Tubing
• B3901882904HRT1: Reprocessed 2.9mm Tricut Blade, Rotatable, with Tubing