Nucleus Removal Cannulas AS13-1601

GUDID 08175700153515

Drews Irrigating Vectis

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: 08175700153515
• NIH Device Record Key: 0d68f892-2870-41a7-b568-aaee56a4701a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nucleus Removal Cannulas
• Version Model Number: AS13-1601
• Catalog Number: AS13-1601
• 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	08175700153515 [Primary]

FDA Product Code

• HMX: Cannula, Ophthalmic

Sterilization

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

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

Moist Heat or Steam Sterilization

[08175700153515]

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

On-Brand Devices [Nucleus Removal Cannulas]

• 08175700153546: Alfonso-McIntyre Irrigating Nucleus Spoon, Large
• 08175700153539: Alfonso-McIntyre Irrigating Nucleus Spoon, Small
• 08175700153522: Sheets Irrigating Vectis
• 08175700153515: Drews Irrigating Vectis
• 08175700153508: Knolle-Pearse Irrigating Vectis
• 08175700153553: Sheets Irrigating Vectis, 23g, Straight, Serrated 6.0mm x 9.0mm Loop, 0.3mm Irrigating Ports