gudid
Primary ID: 8-04-14530-CA
Aurical (UDI 8-04-14530-CA)
Manufactured by Natus Medical Denmark ApS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aurical - Primary ID 8-04-14530-CA
Device Regulatory Overview
The Aurical (Model/Catalog Number: 8-04-14530-CA) is a medical device manufactured by Natus Medical Denmark ApS. This product is indexed under FDA Product Code / Category Classification EWO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8-04-14530-CA
- Product Code / EMDN
- EWO
- Device Name
- 1081 AURICAL AUD with HI-PRO (CA only) Incl. Bone conductor/Insert Phone and TDH Headset
- Database Sync Date
- 2026-08-09 09:12:40
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 Aurical?
The registered manufacturer of record for Aurical is Natus Medical Denmark ApS.
What is the Primary UDI-DI identifier for Aurical?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8-04-14530-CA.
What classification code is assigned to this device?
This device is registered under product classification code EWO.
Similar Classification Devices (EWO)
Other Devices by Natus Medical Denmark ApS
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