AEROSIZER® 90129-501

GUDID 00884450833919

Merit Medical Systems, Inc.

Endoscopic measuring device, pulmonary stricture

• Primary Device ID: 00884450833919
• NIH Device Record Key: d600a4fc-75fe-4bab-b4b3-0b29d37917c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AEROSIZER®
• Version Model Number: D
• Catalog Number: 90129-501
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450833919 [Primary]

FDA Product Code

• FDY: Device, Measuring, For Panendoscope

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-05-20
• Device Publish Date: 2025-05-12

On-Brand Devices [AEROSIZER®]

• 00884450031117: 00884450031117
• 00884450833919: D