eudamed_udi
Primary ID: 06430078510783
BCB Post-monitoring (post-op) Register (UDI 06430078510783)
Manufactured by BCB Medical Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BCB Post-monitoring (post-op) Register - Primary ID 06430078510783
Device Regulatory Overview
The BCB Post-monitoring (post-op) Register (Model/Catalog Number: 06430078510783) 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
- 06430078510783
- Product Code / EMDN
- V92
- Device Name
- Disease Specific Register
- Database Sync Date
- 2026-08-09 18:35:44
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 Post-monitoring (post-op) Register?
The registered manufacturer of record for BCB Post-monitoring (post-op) Register is BCB Medical Oy.
What is the Primary UDI-DI identifier for BCB Post-monitoring (post-op) Register?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430078510783.
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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