Atraumatic Soft Tip VS0210.23

GUDID B384VS0210231

23ga Atraumatic Soft Tip

VORTEX SURGICAL, LLC

Vitrectomy fluid/gas handling handpiece/cannula

• Primary Device ID: B384VS0210231
• NIH Device Record Key: f50e4519-042e-41d8-8f19-6822186617a3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Atraumatic Soft Tip
• Version Model Number: 23ga
• Catalog Number: VS0210.23
• Company DUNS: 080375891
• Company Name: VORTEX 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: 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B384VS0210231 [Primary]

FDA Product Code

• HMX: Cannula, Ophthalmic

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: 2018-09-24
• Device Publish Date: 2018-03-09

On-Brand Devices [Atraumatic Soft Tip]

• B384VS0210251: 25ga Atraumatic Soft Tip
• B384VS0210231: 23ga Atraumatic Soft Tip