eudamed_udi
Primary ID: 07350152820531
VinKep loupes (UDI 07350152820531)
Manufactured by Optergo AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VinKep loupes - Primary ID 07350152820531
Device Regulatory Overview
The VinKep loupes (Model/Catalog Number: 10141) 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
- 10141
- Product Code / EMDN
- Q0299
- Device Name
- Optical Ergonomic Solutions
- Database Sync Date
- 2026-08-09 16:29:13
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 VinKep loupes?
The registered manufacturer of record for VinKep loupes is Optergo AB.
What is the Primary UDI-DI identifier for VinKep loupes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350152820531.
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
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