Meijer

GUDID 00713733546867

Meijer Contact Lens Cases, 12-ct

MEIJER, INC.

Contact lens case

• Primary Device ID: 00713733546867
• NIH Device Record Key: 3e912015-3966-4406-8dae-51528eb9cf58
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Meijer
• Version Model Number: 3637564
• Company DUNS: 006959555
• Company Name: MEIJER, 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: false
• Manufacturing Date: false
• Expiration Date: false
• 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	00713733546867 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K875197

FDA Product Code

• LRX: Case, Contact Lens

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: 2020-05-12
• Device Publish Date: 2020-05-04

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• 10719283500202: Drug Free, Nasal Strips, Clear Extra Strength
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• 10719283500189: Drug Free, Nasal Strips, Tan Extra Strength
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