gudid
Primary ID: BPA-960BT-CA
HOMEDICS (UDI BPA-960BT-CA)
Manufactured by FKA DISTRIBUTING CO., LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HOMEDICS - Primary ID BPA-960BT-CA
Device Regulatory Overview
The HOMEDICS (Model/Catalog Number: BPA-960BT-CA) is a medical device manufactured by FKA DISTRIBUTING CO., LLC. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BPA-960BT-CA
- Product Code / EMDN
- DXN
- Device Name
- PREMIUM ARM BLOOD PRESSURE MONITOR
- Database Sync Date
- 2026-08-09 09:00:32
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 HOMEDICS?
The registered manufacturer of record for HOMEDICS is FKA DISTRIBUTING CO., LLC.
What is the Primary UDI-DI identifier for HOMEDICS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BPA-960BT-CA.
What classification code is assigned to this device?
This device is registered under product classification code DXN.
Similar Classification Devices (DXN)
Other Devices by FKA DISTRIBUTING CO., LLC
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