eudamed_udi Primary ID: 03597610602245

Septaline Instrusept Plus (UDI 03597610602245)

Manufactured by D.M.D.

Data verified against official FDA/EUDAMED records on August 10, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Septaline Instrusept Plus (Model/Catalog Number: 25620922J) 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: 25620922J
Product Code / EMDN: D0901
Device Name: Septaline Instrusept plus 12x1L
Database Sync Date: 2026-08-10 05:06:19

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Septaline Instrusept Plus?

The registered manufacturer of record for Septaline Instrusept Plus is D.M.D..

What is the Primary UDI-DI identifier for Septaline Instrusept Plus?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610602245.

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.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint