eudamed_udi
Primary ID: 06438311036717
TripleAngled BA Excavator3.5mm (UDI 06438311036717)
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 Excavator3.5mm - Primary ID 06438311036717
Device Regulatory Overview
The TripleAngled BA Excavator3.5mm (Model/Catalog Number: 671-681XSI) 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
- 671-681XSI
- Product Code / EMDN
- L159002
- Device Name
- Restorative hand instrument Ir
- 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 TripleAngled BA Excavator3.5mm?
The registered manufacturer of record for TripleAngled BA Excavator3.5mm is LM-Instruments Oy.
What is the Primary UDI-DI identifier for TripleAngled BA Excavator3.5mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438311036717.
What classification code is assigned to this device?
This device is registered under product classification code L159002.
Similar Classification Devices (L159002)
Other Devices by LM-Instruments Oy
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