ASAPLP™ ASAPLP/F

GUDID 10884450511746

Merit Medical Systems, Inc.

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• Primary Device ID: 10884450511746
• NIH Device Record Key: 99bcd1cc-dbaf-4d73-94f7-3916e491226e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASAPLP™
• Version Model Number: 00884450511749
• Catalog Number: ASAPLP/F
• 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: false
• OTC Over-The-Counter: false

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450511749 [Primary]
GS1	10884450511746 [Package]; Contains: 00884450511749; Package: [3 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132155

FDA Product Code

• DXE: Catheter, embolectomy

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: 2021-03-04
• Device Publish Date: 2021-02-24

On-Brand Devices [ASAPLP™]

• 10884450329303: 00884450329306
• 10884450160579: 00884450160572
• 10884450511746: 00884450511749
• 10884450555122: 00884450555125