Amerisource Bergen

GUDID 00368001113052

Non-adherent Pads Sterile 2in X 3in

BP PHARMACEUTICALS LABORATORIES UNLIMITED COMPANY

Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial

• Primary Device ID: 00368001113052
• NIH Device Record Key: cf9d69d1-7ebc-4916-8d84-4f0fb3d65809
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Amerisource Bergen
• Version Model Number: 11305
• Company DUNS: 985523874
• Company Name: BP PHARMACEUTICALS LABORATORIES UNLIMITED COMPANY
• Device Count: 100
• 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: true
• 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	00368001113052 [Primary]
GS1	60368001113054 [Package]; Package: Case [24 Units]; In Commercial Distribution
GS1	80368001113058 [Unit of Use]

FDA Product Code

• NAB: Gauze / Sponge,Nonresorbable For External Use

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-05-28
• Device Publish Date: 2021-05-20

On-Brand Devices [Amerisource Bergen]

• 80368001105473: Face Mask with earloops & Visor Blue, Anti-Fog, Anti-Glare Level3
• 00368001113052: Non-adherent Pads Sterile 2in X 3in
• 00368001113021: Non adherent Pads sterile 3in x 8in
• 00368001113014: Non-adherent Pads Sterile 3in x 4in
• 60368001100528: NITRILE EXAM GLOVES POWDER FREE LILAC COLOUR SIZE: LARGE
• 60368001100511: NITRILE EXAM GLOVES POWDER FREE LILAC COLOUR SIZE: MEDIUM
• 80368001100508: NITRILE EXAM GLOVES POWDER FREE LILAC COLOUR SIZE: SMALL
• 60368001114051: Disposable Underpads Premium 23inX36in ( 58.4gm X 91.4cm)