gudid
Primary ID: AUDIBEL ARIS AI RIC RT
AUDIBEL (UDI AUDIBEL ARIS AI RIC RT)
Manufactured by Starkey Laboratories, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AUDIBEL - Primary ID AUDIBEL ARIS AI RIC RT
Device Regulatory Overview
The AUDIBEL (Model/Catalog Number: AUDIBEL ARIS AI RIC RT) is a medical device manufactured by Starkey Laboratories, Inc.. This product is indexed under FDA Product Code / Category Classification KLW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AUDIBEL ARIS AI RIC RT
- Product Code / EMDN
- KLW
- Device Name
- Database Sync Date
- 2026-08-09 09:07:49
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 AUDIBEL?
The registered manufacturer of record for AUDIBEL is Starkey Laboratories, Inc..
What is the Primary UDI-DI identifier for AUDIBEL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AUDIBEL ARIS AI RIC RT.
What classification code is assigned to this device?
This device is registered under product classification code KLW.
Similar Classification Devices (KLW)
Other Devices by Starkey Laboratories, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint