eudamed_udi
Primary ID: 00842318195425
KINDvaro K400R CROS (UDI 00842318195425)
Manufactured by Starkey Laboratories Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KINDvaro K400R CROS - Primary ID 00842318195425
Device Regulatory Overview
The KINDvaro K400R CROS (Model/Catalog Number: 63332-H23) is a medical device manufactured by Starkey Laboratories Inc.. This product is indexed under FDA Product Code / Category Classification Y2145060102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 63332-H23
- Product Code / EMDN
- Y2145060102
- Device Name
- Genesis AI Standard
- Database Sync Date
- 2026-08-09 16:30:15
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 KINDvaro K400R CROS?
The registered manufacturer of record for KINDvaro K400R CROS is Starkey Laboratories Inc..
What is the Primary UDI-DI identifier for KINDvaro K400R CROS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00842318195425.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060102.
Similar Classification Devices (Y2145060102)
Other Devices by Starkey Laboratories Inc.
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