Datapad

GUDID 04033817900672

LivaNova Deutschland GmbH

Patient health record information system

• Primary Device ID: 04033817900672
• NIH Device Record Key: 8fd5a3c2-d4fa-49a3-b607-2251669705ee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Datapad
• Version Model Number: II
• Company DUNS: 343225272
• Company Name: LivaNova Deutschland GmbH
• 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	04033817900672 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131816

FDA Product Code

• DXJ: DISPLAY, CATHODE-RAY TUBE, MEDICAL

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: 2024-05-07
• Device Publish Date: 2015-10-16

On-Brand Devices [Datapad]

• 04033817901594: DATAPAD III
• 04033817901235: II
• 04033817900689: II
• 04033817900672: II