GUDIDData
eudamed_udi Primary ID: D650020P6020

Splintline Polvere (UDI D650020P6020)

Manufactured by Lang Dental Manufacturing Company, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Splintline Polvere - Primary ID D650020P6020

Device Regulatory Overview

The Splintline Polvere (Model/Catalog Number: 020P602) is a medical device manufactured by Lang Dental Manufacturing Company, Inc.. This product is indexed under FDA Product Code / Category Classification Q010699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
020P602
Product Code / EMDN
Q010699
Device Name
Provisional Crown and Bridge Acrylic
Database Sync Date
2026-08-09 16:28:51

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 Splintline Polvere?

The registered manufacturer of record for Splintline Polvere is Lang Dental Manufacturing Company, Inc..

What is the Primary UDI-DI identifier for Splintline Polvere?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D650020P6020.

What classification code is assigned to this device?

This device is registered under product classification code Q010699.

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