Digital Ultra Package C, International 56200-INT

GUDID 00813830028195

ACCUTRON, INC.

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• Primary Device ID: 00813830028195
• NIH Device Record Key: c98605d9-9b2d-42d3-862a-3c3e72660737
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Digital Ultra Package C, International
• Version Model Number: 56200-INT
• Catalog Number: 56200-INT
• Company DUNS: 088302096
• Company Name: ACCUTRON, 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: true
• 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	00813830028195 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K052335

FDA Product Code

• BSZ: Gas-Machine, Anesthesia

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: 2023-09-21
• Device Publish Date: 2023-09-13

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