GUDIDData
gudid Primary ID: /

SLM Frame & Partial Titanium Alloy (UDI /)

Manufactured by Beijing Yingguan Dental Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SLM Frame & Partial Titanium Alloy - Primary ID /

Device Regulatory Overview

The SLM Frame & Partial Titanium Alloy (Model/Catalog Number: /) is a medical device manufactured by Beijing Yingguan Dental Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NSK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
/
Product Code / EMDN
NSK
Device Name
Database Sync Date
2026-08-09 09:06:36

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of SLM Frame & Partial Titanium Alloy?

The registered manufacturer of record for SLM Frame & Partial Titanium Alloy is Beijing Yingguan Dental Technology Co., Ltd..

What is the Primary UDI-DI identifier for SLM Frame & Partial Titanium Alloy?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is /.

What classification code is assigned to this device?

This device is registered under product classification code NSK.

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