GUDIDData
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gudid Primary ID: 71357005

ANTHOLOGY (UDI 71357005)

Manufactured by Smith & Nephew, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ANTHOLOGY - Primary ID 71357005

Device Regulatory Overview

The ANTHOLOGY (Model/Catalog Number: 71357005) is a medical device manufactured by Smith & Nephew, Inc.. This product is indexed under FDA Product Code / Category Classification MRA 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
Verify if facility inventory is affected by this recall.
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
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
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
71357005
Product Code / EMDN
MRA
Device Name
ANTHOLOGY STANDARD OFFSET POROUS PLUS HYDROXYAPATITE SIZE 5
Database Sync Date
2026-08-09 09:23:32

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 ANTHOLOGY?

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

What is the Primary UDI-DI identifier for ANTHOLOGY?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 71357005.

What classification code is assigned to this device?

This device is registered under product classification code MRA.

Similar Classification Devices (MRA)

Other Devices by Smith & Nephew, Inc.

Programmatic Export

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