GUDIDData
eudamed_udi Primary ID: 04029839987593

5 in 1 System, Größenbest. und Präparation Tibia, Sieb unbestückt (UDI 04029839987593)

Manufactured by Peter Brehm GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 5 in 1 System, Größenbest. und Präparation Tibia, Sieb unbestückt - Primary ID 04029839987593

Device Regulatory Overview

The 5 in 1 System, Größenbest. und Präparation Tibia, Sieb unbestückt (Model/Catalog Number: 98423-30) 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
98423-30
Product Code / EMDN
L091199
Device Name
5 in 1 System, Größenbest. und Präparation Tibia, Sieb unbestückt
Database Sync Date
2026-08-09 16:29:05

Full Regulatory Attributes

🔒 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 5 in 1 System, Größenbest. und Präparation Tibia, Sieb unbestückt?

The registered manufacturer of record for 5 in 1 System, Größenbest. und Präparation Tibia, Sieb unbestückt is Peter Brehm GmbH.

What is the Primary UDI-DI identifier for 5 in 1 System, Größenbest. und Präparation Tibia, Sieb unbestückt?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04029839987593.

What classification code is assigned to this device?

This device is registered under product classification code L091199.

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