Flashpad HD

GUDID 00840682121071

GE MEDICAL SYSTEMS, INC.

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• Primary Device ID: 00840682121071
• NIH Device Record Key: 82118925-3536-4ab2-bd9f-8071aa94fbd8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flashpad HD
• Version Model Number: 4343
• 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	00840682121071 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K172869

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-07-05
• Device Publish Date: 2019-06-27

On-Brand Devices [Flashpad HD]

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