Scleral Depressors AS14-102S

GUDID 08175700156073

O'Connor Scleral Depressor

AURORA SURGICAL, LLC

Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable

• Primary Device ID: 08175700156073
• NIH Device Record Key: 8ae7245d-79d0-4523-89fe-8ea1e4c823ac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Scleral Depressors
• Version Model Number: AS14-102S
• Catalog Number: AS14-102S
• 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	08175700156073 [Primary]

FDA Product Code

• HNX: Depressor, Orbital

Sterilization

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

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

[08175700156073]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-13
• Device Publish Date: 2023-12-05

On-Brand Devices [Scleral Depressors]

• 08175700156103: Spaide Pediatric Scleral Depressor
• 08175700156097: Urretts-Zavalia Depressor and Fixation Pick, Titanium
• 08175700156080: Flynn Scleral Depressor, Stainless Steel
• 08175700156073: O'Connor Scleral Depressor
• 08175700156066: Schepens Scleral Depressor, 12mm, Large
• 08175700156059: Schepens Scleral Depressor, 10mm, Medium
• 08175700156042: Schepens Scleral Depressor, 8mm, Small
• 08175700156035: Flynn Scleral Depressor, Titanium
• 08175700156028: Schocket Double Ended Scleral Depressor, Pediatric, Titanium
• 08175700156011: Schocket Double Ended Scleral Depressor, Adult, Titanium
• 08175700156004: Schocket Double Ended Scleral Depressor, Adult, Stainless Steel
• 08175700156127: Wilder Scleral Depressor, 15mm Tapered Tip, Angled, Titanium
• 08175700156110: O'Connor Scleral Depressor, Titanium