gudid
Primary ID: 8-04-11820
Natus (UDI 8-04-11820)
Manufactured by Natus Medical Denmark ApS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Natus - Primary ID 8-04-11820
Device Regulatory Overview
The Natus (Model/Catalog Number: 8-04-11820) is a medical device manufactured by Natus Medical Denmark ApS. This product is indexed under FDA Product Code / Category Classification ETW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8-04-11820
- Product Code / EMDN
- ETW
- Device Name
- Aurical Freefit with charger (China only)
- Database Sync Date
- 2026-08-09 09:12:40
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Natus?
The registered manufacturer of record for Natus is Natus Medical Denmark ApS.
What is the Primary UDI-DI identifier for Natus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8-04-11820.
What classification code is assigned to this device?
This device is registered under product classification code ETW.
Similar Classification Devices (ETW)
Other Devices by Natus Medical Denmark ApS
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint