SUPERDRY

GUDID 00841543143041

SUNGLASS

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

Spectacle frame

• Primary Device ID: 00841543143041
• NIH Device Record Key: d97e964b-ada9-4cc3-b84a-74ae8645aa11
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SUPERDRY
• Version Model Number: SDS-STUDIOSCREW-272
• 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	00841543143041 [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 [SUPERDRY]

• 00841543143133: SUNGLASS
• 00841543143126: SUNGLASS
• 00841543143089: SUNGLASS
• 00841543143041: SUNGLASS
• 00841543143034: SUNGLASS
• 00841543143027: SUNGLASS
• 00841543143010: SUNGLASS
• 00841543143003: SUNGLASS
• 00841543142990: SUNGLASS
• 00841543142983: SUNGLASS
• 00841543118919: SUNGLASS
• 00841543118902: SUNGLASS
• 00841543118896: SUNGLASS
• 00841543118704: SUNGLASS
• 00841543118698: SUNGLASS
• 00841543118681: SUNGLASS
• 00841543118674: SUNGLASS
• 00841543117219: SUNGLASS
• 00841543112597: SUNGLASS