eudamed_udi
Primary ID: 04051308042687
Valgusplatte (UDI 04051308042687)
Manufactured by Peter Brehm GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Valgusplatte - Primary ID 04051308042687
Device Regulatory Overview
The Valgusplatte (Model/Catalog Number: 42300-836-1) 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
- 42300-836-1
- Product Code / EMDN
- L091199
- Device Name
- BPK-S Integration Instruments
- Database Sync Date
- 2026-08-09 16:30:10
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 Valgusplatte?
The registered manufacturer of record for Valgusplatte is Peter Brehm GmbH.
What is the Primary UDI-DI identifier for Valgusplatte?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04051308042687.
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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