GUDIDData
eudamed_udi Primary ID: 04260181257228

Instru Suc (UDI 04260181257228)

Manufactured by Laboratorium Dr. Deppe GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Instru Suc - Primary ID 04260181257228

Device Regulatory Overview

The Instru Suc (Model/Catalog Number: 601746) is a medical device manufactured by Laboratorium Dr. Deppe GmbH. This product is indexed under FDA Product Code / Category Classification D0901 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
601746
Product Code / EMDN
D0901
Device Name
Instrument Disinfectant
Database Sync Date
2026-08-09 16:50:49

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 Instru Suc?

The registered manufacturer of record for Instru Suc is Laboratorium Dr. Deppe GmbH.

What is the Primary UDI-DI identifier for Instru Suc?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260181257228.

What classification code is assigned to this device?

This device is registered under product classification code D0901.

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