Multi-Purpose Disinfecting Solution

GUDID 00001182254533

RITE AID CORPORATION

Multi-purpose soft/rigid contact lens solution

• Primary Device ID: 00001182254533
• NIH Device Record Key: 9e6ce0a9-0f00-44ed-a348-861210039c70
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Multi-Purpose Disinfecting Solution
• Version Model Number: 049
• Company DUNS: 014578892
• Company Name: RITE AID CORPORATION
• 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: false
• Manufacturing Date: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00001182254533 [Primary]

FDA Product Code

• LPN: Accessories, Soft Lens Products

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-12-18
• Device Publish Date: 2019-12-10

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• 00011822887007 - Rite Aid: 2023-02-17 RA EARLY RST PREG TST 2CT
• 00011822887045 - Rite Aid: 2023-02-17 RA EARLY RSLT PREG TST 3CT
• 00011822887052 - Rite Aid: 2023-02-17 RA DIGITAL PREG TST 2CT
• 00011822887069 - Rite Aid: 2023-02-17 RA ONE STEP PREG TST 2CT
• 00011822887021 - Rite Aid: 2023-02-16 RITE AID +/- PREGNANCY TEST KI