GUDIDData
gudid Primary ID: 1126976

Henry Schein (UDI 1126976)

Manufactured by HENRY SCHEIN, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Henry Schein - Primary ID 1126976

Device Regulatory Overview

The Henry Schein (Model/Catalog Number: 1126976) is a medical device manufactured by HENRY SCHEIN, INC.. This product is indexed under FDA Product Code / Category Classification MED within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1126976
Product Code / EMDN
MED
Device Name
Maxicide OPA 28
Database Sync Date
2026-08-09 09:20:14

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 Henry Schein?

The registered manufacturer of record for Henry Schein is HENRY SCHEIN, INC..

What is the Primary UDI-DI identifier for Henry Schein?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1126976.

What classification code is assigned to this device?

This device is registered under product classification code MED.

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