eudamed_udi
Primary ID: D1231028210
SPATULA (UDI D1231028210)
Manufactured by Dental Expert
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SPATULA - Primary ID D1231028210
Device Regulatory Overview
The SPATULA (Model/Catalog Number: 1028-21) is a medical device manufactured by Dental Expert. This product is indexed under FDA Product Code / Category Classification L159013 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1028-21
- Product Code / EMDN
- L159013
- Device Name
- SPATULA
- Database Sync Date
- 2026-08-09 16:28:47
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 SPATULA?
The registered manufacturer of record for SPATULA is Dental Expert.
What is the Primary UDI-DI identifier for SPATULA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D1231028210.
What classification code is assigned to this device?
This device is registered under product classification code L159013.
Similar Classification Devices (L159013)
Other Devices by Dental Expert
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