eudamed_udi
Primary ID: D123101342B0
EXPLORER (UDI D123101342B0)
Manufactured by Dental Expert
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EXPLORER - Primary ID D123101342B0
Device Regulatory Overview
The EXPLORER (Model/Catalog Number: 1013-42B) is a medical device manufactured by Dental Expert. This product is indexed under FDA Product Code / Category Classification L159003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1013-42B
- Product Code / EMDN
- L159003
- Device Name
- EXPLORER
- Database Sync Date
- 2026-08-09 16:29:28
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 EXPLORER?
The registered manufacturer of record for EXPLORER is Dental Expert.
What is the Primary UDI-DI identifier for EXPLORER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D123101342B0.
What classification code is assigned to this device?
This device is registered under product classification code L159003.
Similar Classification Devices (L159003)
Other Devices by Dental Expert
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