GUDIDData
gudid Primary ID: 20161120

LED NOVA (UDI 20161120)

Manufactured by Karl Storz GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LED NOVA - Primary ID 20161120

Device Regulatory Overview

The LED NOVA (Model/Catalog Number: 20161120) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification NTN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
20161120
Product Code / EMDN
NTN
Device Name
Cold Light Fountain LED nova 100 twin
Database Sync Date
2026-08-09 09:11:33

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 LED NOVA?

The registered manufacturer of record for LED NOVA is Karl Storz GmbH & Co. KG.

What is the Primary UDI-DI identifier for LED NOVA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20161120.

What classification code is assigned to this device?

This device is registered under product classification code NTN.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint