gudid
Primary ID: HX9048/40
Philips Sonicare (UDI HX9048/40)
Manufactured by PHILIPS ORAL HEALTHCARE, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Philips Sonicare - Primary ID HX9048/40
Device Regulatory Overview
The Philips Sonicare (Model/Catalog Number: HX9048/40) is a medical device manufactured by PHILIPS ORAL HEALTHCARE, LLC. This product is indexed under FDA Product Code / Category Classification JEQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HX9048/40
- Product Code / EMDN
- JEQ
- Device Name
- Replacement Brush Head Pack
- Database Sync Date
- 2026-08-09 09:08:46
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 Philips Sonicare?
The registered manufacturer of record for Philips Sonicare is PHILIPS ORAL HEALTHCARE, LLC.
What is the Primary UDI-DI identifier for Philips Sonicare?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HX9048/40.
What classification code is assigned to this device?
This device is registered under product classification code JEQ.
Similar Classification Devices (JEQ)
Other Devices by PHILIPS ORAL HEALTHCARE, LLC
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