ACTU8 Pro-Grip Forceps VS0713.25

GUDID B384VS071325

ACTU8 Pro-Grip 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: B384VS071325
• NIH Device Record Key: 3c1ceef1-0c4c-4aed-98bc-83f34ed56f1a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACTU8 Pro-Grip Forceps
• Version Model Number: Pro-Grip
• Catalog Number: VS0713.25
• 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

Customer Support Contacts

• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com
• Phone: 6367784350
• Email: info@vortexsurgical.com

Device Dimensions

• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B384VS071325 [Primary]

FDA Product Code

• HNR: Forceps, Ophthalmic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-11-12
• Device Publish Date: 2018-10-11

On-Brand Devices [ACTU8 Pro-Grip Forceps]

• B384VS071325: ACTU8 Pro-Grip Forceps
• B384VS071323: ACTU8 Pro-Grip Forceps