eudamed_udi
Primary ID: 06438311208602
Gracey 13/14 SD DTS (UDI 06438311208602)
Manufactured by LM-Instruments Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gracey 13/14 SD DTS - Primary ID 06438311208602
Device Regulatory Overview
The Gracey 13/14 SD DTS (Model/Catalog Number: 213-214SDEST) is a medical device manufactured by LM-Instruments Oy. This product is indexed under FDA Product Code / Category Classification L159001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 213-214SDEST
- Product Code / EMDN
- L159001
- Device Name
- Dental hand instrument, curette for the removal of the supragingival calculus
- Database Sync Date
- 2026-08-09 16:29:14
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 Gracey 13/14 SD DTS?
The registered manufacturer of record for Gracey 13/14 SD DTS is LM-Instruments Oy.
What is the Primary UDI-DI identifier for Gracey 13/14 SD DTS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438311208602.
What classification code is assigned to this device?
This device is registered under product classification code L159001.
Similar Classification Devices (L159001)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint