GUDIDData
eudamed_udi Primary ID: 04260171271661

Bonnets x large (UDI 04260171271661)

Manufactured by Löwenstein Medical SE & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bonnets x large - Primary ID 04260171271661

Device Regulatory Overview

The Bonnets x large (Model/Catalog Number: nj1518-10e) is a medical device manufactured by Löwenstein Medical SE & Co. KG. This product is indexed under FDA Product Code / Category Classification R03010280 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
nj1518-10e
Product Code / EMDN
R03010280
Device Name
Neojet 2000 nCPAP Bonnet
Database Sync Date
2026-08-09 16:28:50

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 Bonnets x large?

The registered manufacturer of record for Bonnets x large is Löwenstein Medical SE & Co. KG.

What is the Primary UDI-DI identifier for Bonnets x large?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260171271661.

What classification code is assigned to this device?

This device is registered under product classification code R03010280.

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