GUDIDData
gudid Primary ID: 15600140 Emerald S Scanner Kit, Cariosity, US

Planmeca Emerald S (UDI 15600140 Emerald S Scanner Kit, Cariosity, US)

Manufactured by D4D TECHNOLOGIES, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Planmeca Emerald S - Primary ID 15600140 Emerald S Scanner Kit, Cariosity, US

Device Regulatory Overview

The Planmeca Emerald S (Model/Catalog Number: 15600140 Emerald S Scanner Kit, Cariosity, US) is a medical device manufactured by D4D TECHNOLOGIES, LLC. This product is indexed under FDA Product Code / Category Classification NTK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
15600140 Emerald S Scanner Kit, Cariosity, US
Product Code / EMDN
NTK
Device Name
Qty 1 - 15610003 - Emerald S Scanner (US)Qty 1 - 15600141 - Emerald S Scanner AccessoriesQty 1 - 15693001 Cariosity Tip
Database Sync Date
2026-08-09 09:49:20

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 Planmeca Emerald S?

The registered manufacturer of record for Planmeca Emerald S is D4D TECHNOLOGIES, LLC.

What is the Primary UDI-DI identifier for Planmeca Emerald S?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15600140 Emerald S Scanner Kit, Cariosity, US.

What classification code is assigned to this device?

This device is registered under product classification code NTK.

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