Victoria Bay

GUDID 00840064620734

Imperial Bag & Paper Co. 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

• Primary Device ID: 00840064620734
• NIH Device Record Key: 3324cad3-d116-4c34-af99-ce8cda7a2f43
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Victoria Bay
• Version Model Number: VBGLN245FML
• Company DUNS: 137977224
• Company Name: Imperial Bag & Paper Co. LLC
• Device Count: 10
• DM Exempt: false
• Pre-market Exempt: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840064620734 [Unit of Use]
GS1	10840064620731 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161944

FDA Product Code

• LZA: Polymer Patient Examination Glove

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: 2023-10-30
• Device Publish Date: 2023-10-20

On-Brand Devices [Victoria Bay]

• 00840064600293: VB-NT-BU
• 00840064600286: VB-NT-BU
• 00840064600279: VB-NT-BU
• 00840064600262: VB-NT-BU
• 00840064600217: VB-NT-BK
• 00840064600200: VB-NT-BK
• 00840064600194: VB-NT-BK
• 00840064600187: VB-NT-BK
• 00840064618748: VB-VY-CL
• 00840064618731: VB-VY-CL
• 00840064618724: VB-VY-CL
• 00840064620789: VBGLN2FXLL
• 00840064620772: VBGLN2FLL
• 00840064620765: VBGLN2FML
• 00840064620758: VBGLN245FXLL
• 00840064620741: VBGLN245FLL
• 00840064620734: VBGLN245FML
• 00840064620642: VBGLN245FSL
• 00840064620635: VBGLN2FSL
• 00840064624336: VBG2N3XL2L
• 00840064624329: VBG2N3L2L
• 00840064624312: VBG2N3M2L
• 00840064624305: VBG2N3S2L