Squirt® FDS100

GUDID 10884450830502

Merit Medical Systems, Inc.

Peripheral vascular intervention infusion catheter

• Primary Device ID: 10884450830502
• NIH Device Record Key: 4ea66dcf-e786-4af6-93c8-b2a5f48de65a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Squirt®
• Version Model Number: A
• Catalog Number: FDS100
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450830505 [Primary]
GS1	10884450830502 [Package]; Contains: 00884450830505; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• KRA: Catheter, continuous flush

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: 2025-04-29
• Device Publish Date: 2025-04-21

On-Brand Devices [Squirt®]

• 10884450045913: 00884450045916
• 10884450830502: A