gudid
Primary ID: STARKEY OMEGA AI CROS RIC 312
STARKEY (UDI STARKEY OMEGA AI CROS RIC 312)
Manufactured by Starkey Laboratories, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STARKEY - Primary ID STARKEY OMEGA AI CROS RIC 312
Device Regulatory Overview
The STARKEY (Model/Catalog Number: STARKEY OMEGA AI CROS RIC 312) 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
- STARKEY OMEGA AI CROS RIC 312
- Product Code / EMDN
- KLW
- Device Name
- Database Sync Date
- 2026-08-09 09:07:49
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 STARKEY?
The registered manufacturer of record for STARKEY is Starkey Laboratories, Inc..
What is the Primary UDI-DI identifier for STARKEY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is STARKEY OMEGA AI CROS RIC 312.
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.
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