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gudid Primary ID: 71270068

VORTEX (UDI 71270068)

Manufactured by Smith & Nephew, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VORTEX - Primary ID 71270068

Device Regulatory Overview

The VORTEX (Model/Catalog Number: 71270068) 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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Unlock Lot Data ($49)
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
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
71270068
Product Code / EMDN
JDZ
Device Name
VORTEX VACUUM BOWL
Database Sync Date
2026-08-09 09:23:34

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 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 71270068.

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.

Programmatic Export

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