eudamed_udi Primary ID: M294CM1723860

EXO-PORT Max, single piece liposuction skin port, Figure 1 (UDI M294CM1723860)

Manufactured by CLINIMED

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EXO-PORT Max, single piece liposuction skin port, Figure 1 (Model/Catalog Number: CM172386) is a medical device manufactured by CLINIMED. This product is indexed under FDA Product Code / Category Classification L250399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CM172386
Product Code / EMDN: L250399
Device Name: EXO-PORT Max, single piece liposuction skin port, Figure 1
Database Sync Date: 2026-08-09 16:45:00

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 EXO-PORT Max, single piece liposuction skin port, Figure 1?

The registered manufacturer of record for EXO-PORT Max, single piece liposuction skin port, Figure 1 is CLINIMED.

What is the Primary UDI-DI identifier for EXO-PORT Max, single piece liposuction skin port, Figure 1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M294CM1723860.

What classification code is assigned to this device?

This device is registered under product classification code L250399.

Similar Classification Devices (L250399)

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