Oasis REST & RELIEF Eye Mask

GUDID 00845819000076

Oasis REST & RELIEF Eye Mask

OASIS MEDICAL, INC.

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• Primary Device ID: 00845819000076
• NIH Device Record Key: 9680bbec-f2b9-445f-a4a2-ada1fc6bfad4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Oasis REST & RELIEF Eye Mask
• Version Model Number: OM8000
• Company DUNS: 194121018
• Company Name: OASIS MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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

Customer Support Contacts

• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00845819000076 [Primary]

FDA Product Code

• IME: Pack, Hot Or Cold, Reusable

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: 2023-07-10
• Device Publish Date: 2023-06-30

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