ReSolve CirQ™ RCQ-10-038MB

GUDID 00884450358900

Merit Medical Systems, Inc.

Closed-wound drain

• Primary Device ID: 00884450358900
• NIH Device Record Key: 2034dee1-0bc3-4cbe-9199-d32ce5ec26b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ReSolve CirQ™
• Version Model Number: 00884450358900
• Catalog Number: RCQ-10-038MB
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 1
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450358900 [Primary]

FDA Product Code

• GBO: CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY

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: 2018-05-18
• Device Publish Date: 2018-04-17

On-Brand Devices [ReSolve CirQ™]

• 00884450400173: 00884450400173
• 00884450358900: 00884450358900