eudamed_udi Primary ID: 03597610612701

SEPTALINE ROTATING PLUS (UDI 03597610612701)

Manufactured by D.M.D.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The SEPTALINE ROTATING PLUS (Model/Catalog Number: 25800472J) is a medical device manufactured by D.M.D.. This product is indexed under FDA Product Code / Category Classification D0901 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 25800472J
Product Code / EMDN: D0901
Device Name: SEPTALINE ROTATING PLUS 5L
Database Sync Date: 2026-08-09 16:47:04

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 SEPTALINE ROTATING PLUS?

The registered manufacturer of record for SEPTALINE ROTATING PLUS is D.M.D..

What is the Primary UDI-DI identifier for SEPTALINE ROTATING PLUS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610612701.

What classification code is assigned to this device?

This device is registered under product classification code D0901.

Similar Classification Devices (D0901)

Other Devices by D.M.D.

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