GUDIDData
Bulk Audit Tool API Access
gudid Primary ID: 71331850

R3 ACETABULAR (UDI 71331850)

Manufactured by Smith & Nephew, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for R3 ACETABULAR - Primary ID 71331850

Device Regulatory Overview

The R3 ACETABULAR (Model/Catalog Number: 71331850) 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
71331850
Product Code / EMDN
MRA
Device Name
R3 0 HOLE ACETABULAR SHELL 50MM
Database Sync Date
2026-08-09 09:23:31

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of R3 ACETABULAR?

The registered manufacturer of record for R3 ACETABULAR is Smith & Nephew, Inc..

What is the Primary UDI-DI identifier for R3 ACETABULAR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 71331850.

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

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint