eudamed_udi
Primary ID: 04029839325685
PROBE TIBIA Komponente SC (UDI 04029839325685)
Manufactured by Peter Brehm GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PROBE TIBIA Komponente SC - Primary ID 04029839325685
Device Regulatory Overview
The PROBE TIBIA Komponente SC (Model/Catalog Number: 42302-205) is a medical device manufactured by Peter Brehm GmbH. This product is indexed under FDA Product Code / Category Classification L091199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 42302-205
- Product Code / EMDN
- L091199
- Device Name
- TRIAL BPK-S Integration
- Database Sync Date
- 2026-08-09 16:29:36
Full Regulatory Attributes
đź”’ Token Gated
{
"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 PROBE TIBIA Komponente SC?
The registered manufacturer of record for PROBE TIBIA Komponente SC is Peter Brehm GmbH.
What is the Primary UDI-DI identifier for PROBE TIBIA Komponente SC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04029839325685.
What classification code is assigned to this device?
This device is registered under product classification code L091199.
Similar Classification Devices (L091199)
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