GUDIDData
gudid Primary ID: 010-009

General Instruments (UDI 010-009)

Manufactured by AMERICAN ORTHODONTICS CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for General Instruments - Primary ID 010-009

Device Regulatory Overview

The General Instruments (Model/Catalog Number: 010-009) is a medical device manufactured by AMERICAN ORTHODONTICS CORPORATION. This product is indexed under FDA Product Code / Category Classification ECP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
010-009
Product Code / EMDN
ECP
Device Name
INSTRUMENT SINGLE END EXPLORER STAINLESS STEEL SPRING WIRE TIP
Database Sync Date
2026-08-09 09:02:46

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 General Instruments?

The registered manufacturer of record for General Instruments is AMERICAN ORTHODONTICS CORPORATION.

What is the Primary UDI-DI identifier for General Instruments?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 010-009.

What classification code is assigned to this device?

This device is registered under product classification code ECP.

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