Under Armour

GUDID 00840331297096

GLACIAL GLASSES, BIFOCAL, .75MM PB EQ

BURLINGTON MEDICAL, LLC

Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles

• Primary Device ID: 00840331297096
• NIH Device Record Key: c650200b-3958-4e50-9d32-5085f3015586
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Under Armour
• Version Model Number: EW-0021-BIF
• 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	00840331297096 [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 [Under Armour]

• 00840331297225: ATTACK 2 GLASSES, PROGRESSIVE, .75MM PB EQ
• 00840331297218: ATTACK 2 GLASSES, BIFOCAL, .75MM PB EQ
• 00840331297201: ATTACK 2 GLASSES, SINGLE VISION, .75MM PB EQ
• 00840331297195: ATTACK 2 GLASSES, NON RX, .75MM PB EQ
• 00840331297102: GLACIAL GLASSES, PROGRESSIVE, .75MM PB EQ
• 00840331297096: GLACIAL GLASSES, BIFOCAL, .75MM PB EQ
• 00840331297089: GLACIAL GLASSES, SINGLE VISION, .75MM PB EQ
• 00840331297072: GLACIAL GLASSES, NON RX, .75MM PB EQ
• 00840331296747: 5043 GLASSES, PROGRESSIVE, .75MM PB EQ
• 00840331296730: 5043 GLASSES, BIFOCAL, .75MM PB EQ
• 00840331296723: 5043 GLASSES, SINGLE VISION, .75MM PB EQ
• 00840331296716: 5043 GLASSES, NON RX, .75MM PB EQ