eudamed_udi
Primary ID: D1231021210
SINUS LIFT EXPLORER (UDI D1231021210)
Manufactured by Dental Expert
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SINUS LIFT EXPLORER - Primary ID D1231021210
Device Regulatory Overview
The SINUS LIFT EXPLORER (Model/Catalog Number: 1021-21) 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
- 1021-21
- Product Code / EMDN
- L159003
- Device Name
- SINUS LIFT EXPLORER
- Database Sync Date
- 2026-08-09 16:28:58
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 SINUS LIFT EXPLORER?
The registered manufacturer of record for SINUS LIFT EXPLORER is Dental Expert.
What is the Primary UDI-DI identifier for SINUS LIFT EXPLORER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D1231021210.
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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