AP Medical

GUDID 00875160007240

AP 30L Duo Bulk P - Wht Blu

Keter Canada Inc

Sharps container

• Primary Device ID: 00875160007240
• NIH Device Record Key: 5c092de3-4aa8-4e17-869f-2112ed86ef2e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AP Medical
• Version Model Number: 242395
• 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	00875160007240 [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