Revolution™ CFG624/D

GUDID 10884450007942

Merit Medical Systems, Inc.

Anaesthesia conduction catheter holder, sterile

• Primary Device ID: 10884450007942
• NIH Device Record Key: ce3a166a-7008-4f9d-9ac7-14a96d90467a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Revolution™
• Version Model Number: 00884450007945
• Catalog Number: CFG624/D
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450007945 [Primary]
GS1	10884450007942 [Package]; Contains: 00884450007945; Package: [25 Units]; In Commercial Distribution

FDA Product Code

• KMK: DEVICE, INTRAVASCULAR CATHETER SECUREMENT

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: 2018-03-29
• Device Publish Date: 2018-02-16

Devices Manufactured by Merit Medical Systems, Inc.

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• 10884450770655 - Performa®: 2024-04-25
• 00884450478264 - Merit Maestro®: 2024-04-24
• 00884450478288 - Merit Maestro®: 2024-04-24
• 10884450697259 - ProGuide™: 2024-04-24
• 10884450712303 - Impress®: 2024-04-24
• 00884450819111 - Merit Medical®: 2024-04-24
• 20884450709188 - Prelude®: 2024-04-24