eudamed_udi
Primary ID: 06430046260757
Optomed Aurora (UDI 06430046260757)
Manufactured by Optomed Oyj
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Optomed Aurora - Primary ID 06430046260757
Device Regulatory Overview
The Optomed Aurora (Model/Catalog Number: 60100635A) is a medical device manufactured by Optomed Oyj. This product is indexed under FDA Product Code / Category Classification Z119003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 60100635A
- Product Code / EMDN
- Z119003
- Device Name
- Aurora full set
- Database Sync Date
- 2026-08-09 17:39:42
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Optomed Aurora?
The registered manufacturer of record for Optomed Aurora is Optomed Oyj.
What is the Primary UDI-DI identifier for Optomed Aurora?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430046260757.
What classification code is assigned to this device?
This device is registered under product classification code Z119003.
Similar Classification Devices (Z119003)
Other Devices by Optomed Oyj
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