Precision

GUDID 00840682119238

GE MEDICAL SYSTEMS, INC.

Stationary general-purpose fluoroscopic x-ray system, digital

• Primary Device ID: 00840682119238
• NIH Device Record Key: 5f22a3ba-f172-45e8-86f5-bf118e2db2f4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Precision
• Version Model Number: 500D
• Company DUNS: 809785715
• Company Name: GE MEDICAL SYSTEMS, INC.
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840682119238 [Primary]

FDA Product Code

• JAA: System, x-ray, fluoroscopic, image-intensified

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: 2016-08-01

On-Brand Devices [Precision]

• 00840682120982: 600FP
• 00840682119238: 500D