Loox

GUDID 00696792096453

Bloom Pink Contact Lens

Camden Passage Inc

Soft corrective contact lens, daily-wear

• Primary Device ID: 00696792096453
• NIH Device Record Key: 1f8d73b2-d5c2-4215-a697-c47eedbd113c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Loox
• Version Model Number: 09.645
• Company DUNS: 250929382
• Company Name: Camden Passage 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00696792096453 [Primary]

FDA Product Code

• LPL: Lenses, Soft Contact, Daily Wear

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: 2024-08-07
• Device Publish Date: 2024-07-30

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