GUDIDData
gudid Primary ID: ES201M

Firefly (UDI ES201M)

Manufactured by Firefly Global

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Firefly - Primary ID ES201M

Device Regulatory Overview

The Firefly (Model/Catalog Number: ES201M) is a medical device manufactured by Firefly Global. This product is indexed under FDA Product Code / Category Classification NTN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ES201M
Product Code / EMDN
NTN
Device Name
Compact handheld light source (battery operated)
Database Sync Date
2026-08-09 09:49:36

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 Firefly?

The registered manufacturer of record for Firefly is Firefly Global.

What is the Primary UDI-DI identifier for Firefly?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ES201M.

What classification code is assigned to this device?

This device is registered under product classification code NTN.

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