Reprocessed 3.4mm Quadcut Blade

GUDID B3901883480HR1

Reprocessed 3.4mm Quadcut Blade, without Tubing

SURETEK MEDICAL

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• Primary Device ID: B3901883480HR1
• NIH Device Record Key: 2aa3a07c-aa82-490f-9241-33c7248feec9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed 3.4mm Quadcut Blade
• Version Model Number: 18-83480HR
• 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	B3901883480HR1 [Primary]

FDA Product Code

• NBH: Accessories, Arthroscopic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-07-04
• Device Publish Date: 2019-05-15

On-Brand Devices [Reprocessed 3.4mm Quadcut Blade]

• B3901883480HRT1: Reprocessed 3.4mm Quadcut Blade, with tubing
• B3901883480HR1: Reprocessed 3.4mm Quadcut Blade, without Tubing