eudamed_udi
Primary ID: 05415174024861
376 (UDI 05415174024861)
Manufactured by Vermeiren Group
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 376 - Primary ID 05415174024861
Device Regulatory Overview
The 376 (Model/Catalog Number: 8000558) is a medical device manufactured by Vermeiren Group. This product is indexed under FDA Product Code / Category Classification Y1803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8000558
- Product Code / EMDN
- Y1803
- Device Name
- 376
- Database Sync Date
- 2026-08-09 16:50:12
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 376?
The registered manufacturer of record for 376 is Vermeiren Group.
What is the Primary UDI-DI identifier for 376?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05415174024861.
What classification code is assigned to this device?
This device is registered under product classification code Y1803.
Similar Classification Devices (Y1803)
Other Devices by Vermeiren Group
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