GUDIDData
eudamed_udi Primary ID: 09551024142548

OROLIN® Multisept Plus (UDI 09551024142548)

Manufactured by United Disinfectant Manufacturers AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OROLIN® Multisept Plus - Primary ID 09551024142548

Device Regulatory Overview

The OROLIN® Multisept Plus (Model/Catalog Number: CH-060020) is a medical device manufactured by United Disinfectant Manufacturers AG. This product is indexed under FDA Product Code / Category Classification D0901 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CH-060020
Product Code / EMDN
D0901
Device Name
Instrument disinfectant
Database Sync Date
2026-08-09 16:30:24

Full Regulatory Attributes

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{
    "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 OROLIN® Multisept Plus?

The registered manufacturer of record for OROLIN® Multisept Plus is United Disinfectant Manufacturers AG.

What is the Primary UDI-DI identifier for OROLIN® Multisept Plus?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09551024142548.

What classification code is assigned to this device?

This device is registered under product classification code D0901.

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