eudamed_udi
Primary ID: 05060031472868
Vellafilm (UDI 05060031472868)
Manufactured by Brightwake Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vellafilm - Primary ID 05060031472868
Device Regulatory Overview
The Vellafilm (Model/Catalog Number: CR3921) is a medical device manufactured by Brightwake Limited. This product is indexed under FDA Product Code / Category Classification M04040701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CR3921
- Product Code / EMDN
- M04040701
- Device Name
- Vellafilm
- Database Sync Date
- 2026-08-09 16:30:42
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 Vellafilm?
The registered manufacturer of record for Vellafilm is Brightwake Limited.
What is the Primary UDI-DI identifier for Vellafilm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060031472868.
What classification code is assigned to this device?
This device is registered under product classification code M04040701.
Similar Classification Devices (M04040701)
Other Devices by Brightwake Limited
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