gudid Primary ID: 71270071

VORTEX (UDI 71270071)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The VORTEX (Model/Catalog Number: 71270071) is a medical device manufactured by Smith & Nephew, Inc.. This product is indexed under FDA Product Code / Category Classification JDZ within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2456-2026 View Full Alert →

TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16, REF: 71760816...

🔒 Compromised Lot & Serial Numbers Locked

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ID: Z-0957-2026 View Full Alert →

BIOSURE HA SCREW, 6MM x 20 MM. Threaded metallic bone fixation fastener....

🔒 Compromised Lot & Serial Numbers Locked

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ID: Z-1806-2025 View Full Alert →

META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690...

🔒 Compromised Lot & Serial Numbers Locked

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Technical Specifications

Model Number: 71270071
Product Code / EMDN: JDZ
Device Name: VORTEX RE-USE KIT
Database Sync Date: 2026-08-09 09:23:36

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 VORTEX?

The registered manufacturer of record for VORTEX is Smith & Nephew, Inc..

What is the Primary UDI-DI identifier for VORTEX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 71270071.

What classification code is assigned to this device?

This device is registered under product classification code JDZ.

Similar Classification Devices (JDZ)

Other Devices by Smith & Nephew, Inc.

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