Reprocessed 2.9mm Quadcut Blade

GUDID B3901882980HR1

Reprocessed 2.9mm Quadcut Blade, without Tubing

SURETEK MEDICAL

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• Primary Device ID: B3901882980HR1
• NIH Device Record Key: 46c1cebb-0978-47fc-a1e6-1fadf37b505f
• Commercial Distribution Discontinuation: 2021-06-14
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Reprocessed 2.9mm Quadcut Blade
• Version Model Number: 18-82980HR
• 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	B3901882980HR1 [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: 2021-06-15
• Device Publish Date: 2019-05-15

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