aries 04000

GUDID 00863897000320

Non-Elevating Radiographic Patient Table HXVF

CORE LABS, LLC

Basic diagnostic x-ray system table, powered

• Primary Device ID: 00863897000320
• NIH Device Record Key: c1f8fb73-4d9b-4123-89d1-ed4cdfb16073
• Commercial Distribution Discontinuation: 2099-12-12
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: aries
• Version Model Number: 04000
• Catalog Number: 04000
• Company DUNS: 622766397
• Company Name: CORE LABS, 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: true
• Manufacturing Date: true
• 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	00863897000320 [Primary]

FDA Product Code

• IXQ: Table, Radiographic, Stationary Top

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-11-17

On-Brand Devices [aries]

• 00863897000320: Non-Elevating Radiographic Patient Table HXVF
• 00863897000313: Non-Elevating Radiographic Patient Table HXVF