gudid
Primary ID: SP101
AURA (UDI SP101)
Manufactured by Branchpoint & Aura Development LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AURA - Primary ID SP101
Device Regulatory Overview
The AURA (Model/Catalog Number: SP101) is a medical device manufactured by Branchpoint & Aura Development LLC. This product is indexed under FDA Product Code / Category Classification GWM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SP101
- Product Code / EMDN
- GWM
- Device Name
- AURA Sensor Tray
- Database Sync Date
- 2026-08-09 09:03:51
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 AURA?
The registered manufacturer of record for AURA is Branchpoint & Aura Development LLC.
What is the Primary UDI-DI identifier for AURA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SP101.
What classification code is assigned to this device?
This device is registered under product classification code GWM.
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