DualCap® 660-DB/A

GUDID 20884450309975

Merit Medical Systems, Inc.

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• Primary Device ID: 20884450309975
• NIH Device Record Key: 31b99a40-93ac-41fb-b45e-9c92797199d4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DualCap®
• Version Model Number: 10884450309978
• Catalog Number: 660-DB/A
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 175
• 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	00884450309971 [Unit of Use]
GS1	10884450309978 [Primary]
GS1	20884450309975 [Package]; Contains: 10884450309978; Package: [6 Units]; In Commercial Distribution

FDA Product Code

• QBP: Cap, device disinfectant

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: 2021-05-25
• Device Publish Date: 2021-05-17

On-Brand Devices [DualCap®]

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