GUDIDData
eudamed_udi Primary ID: 03760124130225

EXTERNAL NEUROLOGICAL DRAINAGE SYSTEM (UDI 03760124130225)

Manufactured by SOPHYSA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EXTERNAL NEUROLOGICAL DRAINAGE SYSTEM - Primary ID 03760124130225

Device Regulatory Overview

The EXTERNAL NEUROLOGICAL DRAINAGE SYSTEM (Model/Catalog Number: DE-210) is a medical device manufactured by SOPHYSA. This product is indexed under FDA Product Code / Category Classification A060399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DE-210
Product Code / EMDN
A060399
Device Name
External Neurological Drainage System
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 EXTERNAL NEUROLOGICAL DRAINAGE SYSTEM?

The registered manufacturer of record for EXTERNAL NEUROLOGICAL DRAINAGE SYSTEM is SOPHYSA.

What is the Primary UDI-DI identifier for EXTERNAL NEUROLOGICAL DRAINAGE SYSTEM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760124130225.

What classification code is assigned to this device?

This device is registered under product classification code A060399.

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