GUDIDData
gudid Primary ID: 996-235CR

Buccal Tubes (UDI 996-235CR)

Manufactured by AMERICAN ORTHODONTICS CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Buccal Tubes - Primary ID 996-235CR

Device Regulatory Overview

The Buccal Tubes (Model/Catalog Number: 996-235CR) is a medical device manufactured by AMERICAN ORTHODONTICS CORPORATION. This product is indexed under FDA Product Code / Category Classification DZD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
996-235CR
Product Code / EMDN
DZD
Device Name
DB TUBE LR 1ST MOL 018/018AUX NON-CONV T-25 R5D 4.2MM W/HK
Database Sync Date
2026-08-09 09:00:41

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 Buccal Tubes?

The registered manufacturer of record for Buccal Tubes is AMERICAN ORTHODONTICS CORPORATION.

What is the Primary UDI-DI identifier for Buccal Tubes?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 996-235CR.

What classification code is assigned to this device?

This device is registered under product classification code DZD.

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