eudamed_udi
Primary ID: 00840388200834
p (UDI 00840388200834)
Manufactured by Starkey Laboratories Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for p - Primary ID 00840388200834
Device Regulatory Overview
The p (Model/Catalog Number: P00002347) is a medical device manufactured by Starkey Laboratories Inc.. This product is indexed under FDA Product Code / Category Classification Y214599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P00002347
- Product Code / EMDN
- Y214599
- Device Name
- Starkey Remote
- Database Sync Date
- 2026-08-09 16:46:06
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 p?
The registered manufacturer of record for p is Starkey Laboratories Inc..
What is the Primary UDI-DI identifier for p?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840388200834.
What classification code is assigned to this device?
This device is registered under product classification code Y214599.
Similar Classification Devices (Y214599)
Other Devices by Starkey Laboratories Inc.
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