ArgoTrans™ 041517504A/A

GUDID 10884450332419

Merit Medical Systems, Inc.

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• Primary Device ID: 10884450332419
• NIH Device Record Key: c6d04628-19fe-4cc5-87f0-ac098b58e65e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ArgoTrans™
• Version Model Number: 10884450332419
• Catalog Number: 041517504A/A
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 20
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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	00884450332412 [Unit of Use]
GS1	10884450332419 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K810637

FDA Product Code

• DRS: Transducer, blood-pressure, extravascular

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: 2019-06-24
• Device Publish Date: 2019-06-14

On-Brand Devices [ArgoTrans™]

• 10884450332815: 10884450332815
• 10884450332419: 10884450332419
• 10884450332372: 10884450332372
• 10884450332488: 10884450332488
• 00884450332825: 10884450332822
• 10884450332839: 10884450332839
• 10884450332549: 10884450332549
• 10884450332532: 10884450332532
• 10884450332525: 10884450332525
• 10884450332518: 10884450332518
• 10884450332501: 10884450332501
• 10884450332495: 10884450332495
• 10884450332433: 10884450332433
• 10884450332426: 10884450332426
• 10884450332389: 10884450332389
• 10884450332341: 10884450332341
• 00884450332801: 10884450332808