gudid Primary ID: CP-5510

Septal-H (UDI CP-5510)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Septal-H (Model/Catalog Number: CP-5510) is a medical device manufactured by SUNMED, LLC. This product is indexed under FDA Product Code / Category Classification FMP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CP-5510
Product Code / EMDN: FMP
Device Name: Septal-H Pediatric Size
Database Sync Date: 2026-08-09 09:04:13

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 Septal-H?

The registered manufacturer of record for Septal-H is SUNMED, LLC.

What is the Primary UDI-DI identifier for Septal-H?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CP-5510.

What classification code is assigned to this device?

This device is registered under product classification code FMP.

Similar Classification Devices (FMP)

Other Devices by SUNMED, LLC

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