gudid
Primary ID: 0290
Circulaire (UDI 0290)
Manufactured by SUNMED, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Circulaire - Primary ID 0290
Device Regulatory Overview
The Circulaire (Model/Catalog Number: 0290) is a medical device manufactured by SUNMED, LLC. This product is indexed under FDA Product Code / Category Classification BYG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0290
- Product Code / EMDN
- BYG
- Device Name
- Circulaire Aerosol Masks
- Database Sync Date
- 2026-08-09 09:04:13
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 Circulaire?
The registered manufacturer of record for Circulaire is SUNMED, LLC.
What is the Primary UDI-DI identifier for Circulaire?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0290.
What classification code is assigned to this device?
This device is registered under product classification code BYG.
Similar Classification Devices (BYG)
Other Devices by SUNMED, LLC
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