eudamed_udi
Primary ID: 04582667981541
EYEVAN (UDI 04582667981541)
Manufactured by EYEVAN Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EYEVAN - Primary ID 04582667981541
Device Regulatory Overview
The EYEVAN (Model/Catalog Number: PUERTO(45)-E 45 PBK) is a medical device manufactured by EYEVAN Inc.. This product is indexed under FDA Product Code / Category Classification Q02100202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PUERTO(45)-E 45 PBK
- Product Code / EMDN
- Q02100202
- Device Name
- Plastic spectacle frames without lenses
- Database Sync Date
- 2026-08-09 16:29:32
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 EYEVAN?
The registered manufacturer of record for EYEVAN is EYEVAN Inc..
What is the Primary UDI-DI identifier for EYEVAN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04582667981541.
What classification code is assigned to this device?
This device is registered under product classification code Q02100202.
Similar Classification Devices (Q02100202)
Other Devices by EYEVAN Inc.
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