gudid
Primary ID: BH1021/09
Philips One (UDI BH1021/09)
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 One - Primary ID BH1021/09
Device Regulatory Overview
The Philips One (Model/Catalog Number: BH1021/09) 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
- BH1021/09
- Product Code / EMDN
- JEQ
- Device Name
- Database Sync Date
- 2026-08-09 09:08:46
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Philips One?
The registered manufacturer of record for Philips One is PHILIPS ORAL HEALTHCARE, LLC.
What is the Primary UDI-DI identifier for Philips One?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BH1021/09.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint