DualCap® 001-300/A

GUDID 20884450309418

Merit Medical Systems, Inc.

Luer-formatted disinfectant cap

• Primary Device ID: 20884450309418
• NIH Device Record Key: 8691400b-04e2-4a1f-addf-c12f9d34d278
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DualCap®
• Version Model Number: 10884450309411
• Catalog Number: 001-300/A
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 350
• 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: false
• Expiration Date: true
• 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	00884450309414 [Unit of Use]
GS1	10884450309411 [Primary]
GS1	20884450309418 [Package]; Contains: 10884450309411; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• LKB: Pad, alcohol, device disinfectant
• QBP: Cap, device disinfectant

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-08-07
• Device Publish Date: 2018-09-28

On-Brand Devices [DualCap®]

• 20884450309456: 10884450309459
• 20884450390737: 10884450390730
• 20884450309425: 10884450309428
• 20884450309418: 10884450309411
• 20884450309371: 10884450309374
• 20884450309364: 10884450309367
• 20884450309975: 10884450309978