GUDIDData
eudamed_udi Primary ID: 04051308032466

PROBE ADAPTER Femur SC + RH + TH (UDI 04051308032466)

Manufactured by Peter Brehm GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PROBE ADAPTER Femur SC + RH + TH - Primary ID 04051308032466

Device Regulatory Overview

The PROBE ADAPTER Femur SC + RH + TH (Model/Catalog Number: 42705-252) 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
42705-252
Product Code / EMDN
L091199
Device Name
TRIAL BPK-S Integration
Database Sync Date
2026-08-09 16:29:05

Full Regulatory Attributes

đź”’ Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of PROBE ADAPTER Femur SC + RH + TH?

The registered manufacturer of record for PROBE ADAPTER Femur SC + RH + TH is Peter Brehm GmbH.

What is the Primary UDI-DI identifier for PROBE ADAPTER Femur SC + RH + TH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04051308032466.

What classification code is assigned to this device?

This device is registered under product classification code L091199.

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