Front Line

GUDID 00814889014207

FINGERCOTS LG BLUE

Prostat First Aid, LLC

Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 00814889014207
• NIH Device Record Key: 37b62e7e-3e79-4766-980a-ea38e37618c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Front Line
• Version Model Number: 2436
• Company DUNS: 117129815
• Company Name: Prostat First Aid, 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: true
• Lot Batch: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814889014207 [Primary]

FDA Product Code

• LZB: Finger Cot

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: 2022-11-07
• Device Publish Date: 2022-10-28

On-Brand Devices [Front Line]

• 00814889010025: BLUE WOVEN FINGERTIP BANDAGE
• 00814889010018: BLUE WOVEN KNUCKLE BANDAGE
• 00814889010001: BLUE WOVEN ADHESIVE BANDAGE 1" X 3"
• 00814889014207: FINGERCOTS LG BLUE
• 00814889014160: FINGERCOTS MD BLUE
• 00814889014153: FINGERCOTS LG BLUE
• 00814889013781: FINGERCOTS MD BLUE
• 00814889013323: FLS BLUE FINGERTIP
• 00814889013316: FL BLUE WOVEN KNUCKLE
• 00814889013309: FL BLUE WOVEN 1" x 3"
• 00814889010377: FINGERCOTS MD BLUE
• 00814889014832: COLD PACK 5" x 6" BULK
• 00814889014825: ELASTIC BANDAGE 3"X5YD
• 00814889014818: COLD PACK 5" x 6" BOXED
• 00814889014801: SELF ADHERENT WRAP BLUE 2"X5YD
• 00814889014795: Gauze Roll 3" NS
• 00814889014788: WHT ADHESIVE TRI-CUT TAPE
• 00814889014771: GAUZE PADS STERILE 3"X3"
• 00814889014924: Dressing Burn Gel 4"x4"