eudamed_udi
Primary ID: 06438311036342
TripleAngled BA Excavator1.5mm DTS (UDI 06438311036342)
Manufactured by LM-Instruments Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TripleAngled BA Excavator1.5mm DTS - Primary ID 06438311036342
Device Regulatory Overview
The TripleAngled BA Excavator1.5mm DTS (Model/Catalog Number: 631-641EST) is a medical device manufactured by LM-Instruments Oy. This product is indexed under FDA Product Code / Category Classification L159002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 631-641EST
- Product Code / EMDN
- L159002
- Device Name
- Dental hand instrument, excavator for the removal of softened carious dentin
- Database Sync Date
- 2026-08-09 16:46:25
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 TripleAngled BA Excavator1.5mm DTS?
The registered manufacturer of record for TripleAngled BA Excavator1.5mm DTS is LM-Instruments Oy.
What is the Primary UDI-DI identifier for TripleAngled BA Excavator1.5mm DTS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438311036342.
What classification code is assigned to this device?
This device is registered under product classification code L159002.
Similar Classification Devices (L159002)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint