eudamed_udi
Primary ID: 00840388202500
KINDsignature 3 CIC NW (UDI 00840388202500)
Manufactured by Starkey Laboratories Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KINDsignature 3 CIC NW - Primary ID 00840388202500
Device Regulatory Overview
The KINDsignature 3 CIC NW (Model/Catalog Number: P00004247) is a medical device manufactured by Starkey Laboratories Inc.. This product is indexed under FDA Product Code / Category Classification Y2145060203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P00004247
- Product Code / EMDN
- Y2145060203
- Device Name
- Signature Series Custom
- Database Sync Date
- 2026-08-09 16:47:04
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 KINDsignature 3 CIC NW?
The registered manufacturer of record for KINDsignature 3 CIC NW is Starkey Laboratories Inc..
What is the Primary UDI-DI identifier for KINDsignature 3 CIC NW?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840388202500.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060203.
Similar Classification Devices (Y2145060203)
Other Devices by Starkey Laboratories Inc.
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