GUDID 10856602005069

PROTEUS DIGITAL HEALTH, INC.

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• Primary Device ID: 10856602005069
• NIH Device Record Key: f275d4ff-7566-4fdf-9fe8-4c785b72997a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: SPC-0572.B59
• Company DUNS: 149825791
• Company Name: PROTEUS DIGITAL HEALTH, INC.
• Device Count: 450
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	00856602005062 [Unit of Use]
GS1	10856602005069 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133263

FDA Product Code

• OZW: Ingestible event marker

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: 2022-11-28
• Device Publish Date: 2016-07-07

Devices Manufactured by PROTEUS DIGITAL HEALTH, INC.

• 10856602005021 - NA: 2022-11-28
• 10856602005045 - NA: 2022-11-28
• 10856602005052 - NA: 2022-11-28
• 10856602005069 - NA: 2022-11-28
• 10856602005069 - NA: 2022-11-28
• 10856602005076 - NA: 2022-11-28
• 10856602005083 - NA: 2022-11-28
• 10856602005090 - NA: 2022-11-28
• 10856602005106 - NA: 2022-11-28