eudamed_udi
Primary ID: 07350152820197
Ultralight Flip-up loupes (UDI 07350152820197)
Manufactured by Optergo AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ultralight Flip-up loupes - Primary ID 07350152820197
Device Regulatory Overview
The Ultralight Flip-up loupes (Model/Catalog Number: 10131) is a medical device manufactured by Optergo AB. This product is indexed under FDA Product Code / Category Classification Q0299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10131
- Product Code / EMDN
- Q0299
- Device Name
- Optical Ergonomic Solutions
- Database Sync Date
- 2026-08-09 16:46:28
Full Regulatory Attributes
🔒 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 Ultralight Flip-up loupes?
The registered manufacturer of record for Ultralight Flip-up loupes is Optergo AB.
What is the Primary UDI-DI identifier for Ultralight Flip-up loupes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350152820197.
What classification code is assigned to this device?
This device is registered under product classification code Q0299.
Similar Classification Devices (Q0299)
Other Devices by Optergo AB
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint