Gimmi (UDI E.8300.48 LED)

Manufactured by Gimmi GmbH

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Gimmi (Model/Catalog Number: E.8300.48 LED) is a medical device manufactured by Gimmi GmbH. This product is indexed under FDA Product Code / Category Classification NTN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: E.8300.48 LED
Product Code / EMDN: NTN
Device Name: FIBRE OPTIC LIGHT CABLE FOR LED 4.8 MM, WITHOUT ADAPTERSLENGTH 300 CM
Database Sync Date: 2026-08-09 09:11:28

Full Regulatory Attributes

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{
    "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 Gimmi?

The registered manufacturer of record for Gimmi is Gimmi GmbH.

What is the Primary UDI-DI identifier for Gimmi?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E.8300.48 LED.

What classification code is assigned to this device?

This device is registered under product classification code NTN.

Similar Classification Devices (NTN)

Other Devices by Gimmi GmbH

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