GUDIDData
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gudid Primary ID: 71271440

VERSABOND (UDI 71271440)

Manufactured by Smith & Nephew, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VERSABOND - Primary ID 71271440

Device Regulatory Overview

The VERSABOND (Model/Catalog Number: 71271440) is a medical device manufactured by Smith & Nephew, Inc.. This product is indexed under FDA Product Code / Category Classification LOD 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
Verify if facility inventory is affected by this recall.
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Technical Specifications

Model Number
71271440
Product Code / EMDN
LOD
Device Name
VERSABOND AB 40 GRAMS FORMULATION 2
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 VERSABOND?

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

What is the Primary UDI-DI identifier for VERSABOND?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 71271440.

What classification code is assigned to this device?

This device is registered under product classification code LOD.

Similar Classification Devices (LOD)

Other Devices by Smith & Nephew, Inc.

Programmatic Export

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