GUDIDData
gudid Primary ID: 1 016

N/A (UDI 1 016)

Manufactured by Zimmer, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID 1 016

Device Regulatory Overview

The N/A (Model/Catalog Number: 1 016) is a medical device manufactured by Zimmer, Inc.. This product is indexed under FDA Product Code / Category Classification EJL 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-2578-2026 View Full Alert →

Brand Name: Persona Revision Product Name: Persona Revision Trabecular Metal Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 ...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2529-2026 View Full Alert →

Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040242...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2531-2026 View Full Alert →

Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040476...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
1 016
Product Code / EMDN
EJL
Device Name
Rotary steel instrument for dental application
Database Sync Date
2026-08-09 09:01:02

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 N/A?

The registered manufacturer of record for N/A is Zimmer, Inc..

What is the Primary UDI-DI identifier for N/A?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1 016.

What classification code is assigned to this device?

This device is registered under product classification code EJL.

Programmatic Export

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

JSON API Endpoint