Athelas Home

GUDID 00860008385864

Athelas, Inc.

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• Primary Device ID: 00860008385864
• NIH Device Record Key: 03ed84a8-eaff-4b70-af27-108ca346009c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Athelas Home
• Version Model Number: 850-00002-00
• Company DUNS: 080636378
• Company Name: Athelas, Inc.
• Device Count: 50
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860008385864 [Unit of Use]
GS1	20860008385868 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K200828

FDA Product Code

• GKZ: Counter, Differential Cell

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: 2022-08-08
• Device Publish Date: 2022-07-29

On-Brand Devices [Athelas Home]

• 00860008385864: 850-00002-00
• 00860008385840: 850-00001-00