GUDIDData
eudamed_udi Primary ID: 05060511622462

MAXI HME Pleat (UDI 05060511622462)

Manufactured by GVS Filter Technology UK Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MAXI HME Pleat - Primary ID 05060511622462

Device Regulatory Overview

The MAXI HME Pleat (Model/Catalog Number: 4244/711BRSA066/0001) is a medical device manufactured by GVS Filter Technology UK Limited. This product is indexed under FDA Product Code / Category Classification R040102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
4244/711BRSA066/0001
Product Code / EMDN
R040102
Device Name
Humidification Systems
Database Sync Date
2026-08-09 16:47:15

Full Regulatory Attributes

🔒 Token Gated
{
    "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 MAXI HME Pleat?

The registered manufacturer of record for MAXI HME Pleat is GVS Filter Technology UK Limited.

What is the Primary UDI-DI identifier for MAXI HME Pleat?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060511622462.

What classification code is assigned to this device?

This device is registered under product classification code R040102.

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