REEL LEGENDS

GUDID 00841543135565

SUNGLASS

Inspecs U.S.A., L.C.

Spectacle frame

• Primary Device ID: 00841543135565
• NIH Device Record Key: a30253a2-67e9-47f9-854e-7fa78c1cb2b1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REEL LEGENDS
• Version Model Number: BRS-MONTAUK-127P
• Company DUNS: 845937478
• Company Name: Inspecs U.S.A., L.C.
• 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: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841543135565 [Primary]

FDA Product Code

• HQY: Sunglasses (non-prescription including photosensitive)

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: 2022-12-09
• Device Publish Date: 2022-12-01

On-Brand Devices [REEL LEGENDS]

• 00841543135589: SUNGLASS
• 00841543135565: SUNGLASS
• 00841543135534: SUNGLASS