GUDIDData
eudamed_udi Primary ID: 06430046261006

Optomed Smartscope (UDI 06430046261006)

Manufactured by Optomed Oyj

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Optomed Smartscope - Primary ID 06430046261006

Device Regulatory Overview

The Optomed Smartscope (Model/Catalog Number: 41000040) is a medical device manufactured by Optomed Oyj. This product is indexed under FDA Product Code / Category Classification Z119007 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
41000040
Product Code / EMDN
Z119007
Device Name
Smartscope FA optics
Database Sync Date
2026-08-09 16:45:43

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 Optomed Smartscope?

The registered manufacturer of record for Optomed Smartscope is Optomed Oyj.

What is the Primary UDI-DI identifier for Optomed Smartscope?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430046261006.

What classification code is assigned to this device?

This device is registered under product classification code Z119007.

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