Venue Fit

GUDID 00195278703484

Venue Fit R5 MD

GE MEDICAL SYSTEMS, ULTRASOUND & PRIMARY CARE DIAGNOSTICS, LLC

General-purpose ultrasound imaging system

• Primary Device ID: 00195278703484
• NIH Device Record Key: fe9b6f72-5995-4463-93dc-d4b5b14ab8e5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Venue Fit
• Version Model Number: R5 UPG
• Company DUNS: 078863378
• Company Name: GE MEDICAL SYSTEMS, ULTRASOUND & PRIMARY CARE DIAGNOSTICS, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00195278703484 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K234106

FDA Product Code

• ITX: Transducer, ultrasonic, diagnostic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-18
• Device Publish Date: 2024-07-10

On-Brand Devices [Venue Fit]

• 00195278194275: Venue Fit final Assy.
• 00195278516497: Venue Fit R4 Final Assembly
• 00195278513014: Venue Fit R4 MD either eDelivery or physical
• 00195278703484: Venue Fit R5 MD
• 00195278703224: Venue Fit R5 Final Assembly