DualCap® 550-LB/A

GUDID 20884450309456

Merit Medical Systems, Inc.

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• Primary Device ID: 20884450309456
• NIH Device Record Key: 3d5de113-40c5-4f47-aea1-c4c65ad6a54f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DualCap®
• Version Model Number: 10884450309459
• Catalog Number: 550-LB/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	00884450309452 [Unit of Use]
GS1	10884450309459 [Primary]
GS1	20884450309456 [Package]; Contains: 10884450309459; Package: [12 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: 2020-01-14
• Device Publish Date: 2020-01-06

On-Brand Devices [DualCap®]

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