pma Primary ID: P940016

H.E.L.P. SYSTEM (UDI P940016)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The H.E.L.P. SYSTEM (Model/Catalog Number: Unspecified) is a medical device manufactured by B. Braun Avitum AG. This product is indexed under FDA Product Code / Category Classification MMY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: N/A
Product Code / EMDN: MMY
Device Name: Lipoprotein, low density, removal
Database Sync Date: 2026-08-09 10:06:22

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 H.E.L.P. SYSTEM?

The registered manufacturer of record for H.E.L.P. SYSTEM is B. Braun Avitum AG.

What is the Primary UDI-DI identifier for H.E.L.P. SYSTEM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P940016.

What classification code is assigned to this device?

This device is registered under product classification code MMY.

Similar Classification Devices (MMY)

Other Devices by B. Braun Avitum AG

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