GUDIDData
gudid Primary ID: X1L001

NATUS NEUROLOGY (UDI X1L001)

Manufactured by NATUS NEUROLOGY INCORPORATED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NATUS NEUROLOGY - Primary ID X1L001

Device Regulatory Overview

The NATUS NEUROLOGY (Model/Catalog Number: X1L001) is a medical device manufactured by NATUS NEUROLOGY INCORPORATED. This product is indexed under FDA Product Code / Category Classification JAF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
X1L001
Product Code / EMDN
JAF
Device Name
ELITE 3MHZ OB PROBE
Database Sync Date
2026-08-09 10:02:47

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 NATUS NEUROLOGY?

The registered manufacturer of record for NATUS NEUROLOGY is NATUS NEUROLOGY INCORPORATED.

What is the Primary UDI-DI identifier for NATUS NEUROLOGY?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is X1L001.

What classification code is assigned to this device?

This device is registered under product classification code JAF.

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