ACTU8 Tewari (T2) Forceps VS0742.25

GUDID B384VS074225

Ophthalmic Forceps

VORTEX SURGICAL, LLC

Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use

• Primary Device ID: B384VS074225
• NIH Device Record Key: 5dcf5a68-8a6a-49a8-9eeb-90699553c747
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACTU8 Tewari (T2) Forceps
• Version Model Number: 25ga
• Catalog Number: VS0742.25
• 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	B384VS074225 [Primary]

FDA Product Code

• HNR: Forceps, 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: 3
• Public Version Date: 2018-10-05
• Device Publish Date: 2018-03-15

On-Brand Devices [ACTU8 Tewari (T2) Forceps]

• B384VS074225: Ophthalmic Forceps
• B384VS074221: Ophthalmic Forceps