Haven

GUDID 00840331296396

LSND FITOVER GLASSES, NON RX, .75MM PB EQ

BURLINGTON MEDICAL, LLC

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• Primary Device ID: 00840331296396
• NIH Device Record Key: 10f7b682-4bb5-4bb9-8db1-3588f25f7d82
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Haven
• Version Model Number: EW-0003-NONRX
• Company DUNS: 083381202
• Company Name: BURLINGTON MEDICAL, LLC
• 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: false
• Lot Batch: true
• Serial Number: true
• 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	00840331296396 [Primary]

FDA Product Code

• IWS: Shield, Eye, Radiological

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: 2024-04-22
• Device Publish Date: 2024-04-12

On-Brand Devices [Haven]

• 00840331296426: LSND FITOVER GLASSES, PROGRESSIVE, .75MM PB EQ
• 00840331296419: LSND FITOVER GLASSES, BIFOCAL, .75MM PB EQ
• 00840331296402: LSND FITOVER GLASSES, SINGLE VISION, .75MM PB EQ
• 00840331296396: LSND FITOVER GLASSES, NON RX, .75MM PB EQ