Cortex Extractors AS13-1300-13/21g

GUDID 08175700152006

Simcoe Cortex Extractor Cannula, 13/21 mm

AURORA SURGICAL, LLC

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable

• Primary Device ID: 08175700152006
• NIH Device Record Key: 70e004d1-a675-4a2a-827e-9b74280c3c72
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cortex Extractors
• Version Model Number: AS13-1300-13/21g
• Catalog Number: AS13-1300-13/21g
• Company DUNS: 968368832
• Company Name: AURORA SURGICAL, LLC
• 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: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08175700152006 [Primary]

FDA Product Code

• HMX: Cannula, Ophthalmic

Sterilization

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

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

[08175700152006]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-07-25
• Device Publish Date: 2023-07-17

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