eudamed_udi
Primary ID: 06430046262300
Optomed Smartscope (UDI 06430046262300)
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 06430046262300
Device Regulatory Overview
The Optomed Smartscope (Model/Catalog Number: 41000032) is a medical device manufactured by Optomed Oyj. This product is indexed under FDA Product Code / Category Classification Z119080 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 41000032
- Product Code / EMDN
- Z119080
- Device Name
- Smartscope Cradle V1
- Database Sync Date
- 2026-08-09 17:41:00
Full Regulatory Attributes
đź”’ 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 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 06430046262300.
What classification code is assigned to this device?
This device is registered under product classification code Z119080.
Similar Classification Devices (Z119080)
Other Devices by Optomed Oyj
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint