RADLEY

GUDID 00841543131222

SUNGLASS

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

Spectacle frame

• Primary Device ID: 00841543131222
• NIH Device Record Key: 620ccc44-c58d-462d-b661-b047d87dccb3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RADLEY
• Version Model Number: RDS-TULIP-161
• 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	00841543131222 [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 [RADLEY]

• 00841543143614: SUNGLASS
• 00841543143591: SUNGLASS
• 00841543143584: SUNGLASS
• 00841543131222: SUNGLASS
• 00841543131215: SUNGLASS