Phoenix Neuro (UDI SRS09)

Manufactured by SOPHYSA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Phoenix Neuro (Model/Catalog Number: SRS09) is a medical device manufactured by SOPHYSA. This product is indexed under FDA Product Code / Category Classification JXG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SRS09
Product Code / EMDN: JXG
Device Name: Endoscopic right angle, AB ventricular catheter with reservoir, 9 cm
Database Sync Date: 2026-08-09 09:33:52

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 Phoenix Neuro?

The registered manufacturer of record for Phoenix Neuro is SOPHYSA.

What is the Primary UDI-DI identifier for Phoenix Neuro?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SRS09.

What classification code is assigned to this device?

This device is registered under product classification code JXG.

Similar Classification Devices (JXG)

Other Devices by SOPHYSA

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