Flashpad HD

GUDID 00840682120807

GE MEDICAL SYSTEMS, INC.

Indirect flat panel x-ray detector

• Primary Device ID: 00840682120807
• NIH Device Record Key: eb1cf74e-31c6-475c-a711-93f1abd7848f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flashpad HD
• Version Model Number: 3543
• 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	00840682120807 [Primary]

FDA Product Code

• MQB: Solid state x-ray imager (flat panel/digital imager)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-05-07
• Device Publish Date: 2017-07-28

On-Brand Devices [Flashpad HD]

• 00840682120807: 3543
• 00840682120784: 2530
• 00840682121071: 4343