eudamed_udi
Primary ID: 06430078510714
BCB Vascular procedures, vena Register (UDI 06430078510714)
Manufactured by BCB Medical Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BCB Vascular procedures, vena Register - Primary ID 06430078510714
Device Regulatory Overview
The BCB Vascular procedures, vena Register (Model/Catalog Number: 06430078510714) is a medical device manufactured by BCB Medical Oy. This product is indexed under FDA Product Code / Category Classification V92 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 06430078510714
- Product Code / EMDN
- V92
- Device Name
- Disease Specific Register
- Database Sync Date
- 2026-08-09 17:33:31
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 BCB Vascular procedures, vena Register?
The registered manufacturer of record for BCB Vascular procedures, vena Register is BCB Medical Oy.
What is the Primary UDI-DI identifier for BCB Vascular procedures, vena Register?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430078510714.
What classification code is assigned to this device?
This device is registered under product classification code V92.
Similar Classification Devices (V92)
Other Devices by BCB Medical Oy
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