AP Medical

GUDID 00875160007226

AP 50L Duo Bulk Wht Blu

Keter Canada Inc

Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container

• Primary Device ID: 00875160007226
• NIH Device Record Key: 1651c538-7eb6-4106-96b6-aa9a2c657e14
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AP Medical
• Version Model Number: 242508
• 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	00875160007226 [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 [AP Medical]

• 00875160007318: AP 50L Duo Bulk Wht Blu
• 00875160007240: AP 30L Duo Bulk P - Wht Blu
• 00875160007226: AP 50L Duo Bulk Wht Blu