BD 259866

GUDID 00990013400099

Becton Dickinson - AP 60 DUO BLACK

Keter Canada Inc

Sharps container

• Primary Device ID: 00990013400099
• NIH Device Record Key: 3a63006a-d0be-4641-9ccf-41b866f4e570
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD
• Version Model Number: 304462
• Catalog Number: 259866
• Company DUNS: 253548978
• Company Name: Keter Canada Inc
• Device Count: 1
• 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: 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	00990013400099 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071517

FDA Product Code

• MMK: Container, Sharps

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: 2024-05-23
• Device Publish Date: 2024-05-15

On-Brand Devices [BD]

• 00990013400136: Becton Dickinson - AP 30 DUO BLACK
• 00990013400129: Becton Dickinson - AP 30 DUO WHITE
• 00990013400112: Becton Dickinson - AP 30 DUO YELLOW
• 00990013400105: Becton Dickinson - AP 30 DUO RED
• 00990013400099: Becton Dickinson - AP 60 DUO BLACK
• 00990013400082: Becton Dickinson - AP 60 DUO WHITE
• 00990013400075: Becton Dickinson - AP 60 DUO YELLOW
• 00990013400068: Becton Dickinson - AP 60 DUO RED