eudamed_udi
Primary ID: 03770037649004
AURORIA (UDI 03770037649004)
Manufactured by MIST STUDIO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AURORIA - Primary ID 03770037649004
Device Regulatory Overview
The AURORIA (Model/Catalog Number: AURORIA) is a medical device manufactured by MIST STUDIO. This product is indexed under FDA Product Code / Category Classification V92 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AURORIA
- Product Code / EMDN
- V92
- Device Name
- AURORIA
- Database Sync Date
- 2026-08-09 16:28:45
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 AURORIA?
The registered manufacturer of record for AURORIA is MIST STUDIO.
What is the Primary UDI-DI identifier for AURORIA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03770037649004.
What classification code is assigned to this device?
This device is registered under product classification code V92.
Similar Classification Devices (V92)
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