Aspira (UDI Initial Release)
Manufactured by Merit Medical Systems, Inc.
Device Regulatory Overview
The Aspira (Model/Catalog Number: Initial Release) is a medical device manufactured by Merit Medical Systems, Inc.. This product is indexed under FDA Product Code / Category Classification DWM within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- Initial Release
- Product Code / EMDN
- DWM
- Device Name
- Database Sync Date
- 2026-08-09 09:45:43
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Aspira?
The registered manufacturer of record for Aspira is Merit Medical Systems, Inc..
What is the Primary UDI-DI identifier for Aspira?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Initial Release.
What classification code is assigned to this device?
This device is registered under product classification code DWM.
Similar Classification Devices (DWM)
Other Devices by Merit Medical Systems, Inc.
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JSON API Endpoint