GUDIDData
gudid Primary ID: 112

Denture, Restoration (UDI 112)

Manufactured by ACESO DENTAL LABORATORY COMPANY LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Denture, Restoration - Primary ID 112

Device Regulatory Overview

The Denture, Restoration (Model/Catalog Number: 112) is a medical device manufactured by ACESO DENTAL LABORATORY COMPANY LIMITED. This product is indexed under FDA Product Code / Category Classification NSJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
112
Product Code / EMDN
NSJ
Device Name
Database Sync Date
2026-08-09 09:29:37

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 Denture, Restoration?

The registered manufacturer of record for Denture, Restoration is ACESO DENTAL LABORATORY COMPANY LIMITED.

What is the Primary UDI-DI identifier for Denture, Restoration?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 112.

What classification code is assigned to this device?

This device is registered under product classification code NSJ.

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