gudid Primary ID: 88602

Galaxy (UDI 88602)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Galaxy (Model/Catalog Number: 88602) is a medical device manufactured by Ortho Organizers, Inc.. This product is indexed under FDA Product Code / Category Classification EHM within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 2 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2477-2020 View Full Alert →

Maestro Orthodontic Bracket REF711-206-10 QTY. 10 Rx Only (01)00190707016517 (10)112233 (422)484...

🔒 Compromised Lot & Serial Numbers Locked

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ID: Z-2478-2020 View Full Alert →

Maestro Orthodontic Bracket REF711-298Q QTY. 20 Rx Only (01)00190707017064 (10)889437 (422)484 Maestro Orthodontic Bracket REF711-299MCQ...

🔒 Compromised Lot & Serial Numbers Locked

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Technical Specifications

Model Number: 88602
Product Code / EMDN: EHM
Device Name: GALAXY Perforated Strips Narrow Fine 10/pk 2.5mm wide 30 micron
Database Sync Date: 2026-08-09 09:00:45

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 Galaxy?

The registered manufacturer of record for Galaxy is Ortho Organizers, Inc..

What is the Primary UDI-DI identifier for Galaxy?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 88602.

What classification code is assigned to this device?

This device is registered under product classification code EHM.

Similar Classification Devices (EHM)

Other Devices by Ortho Organizers, Inc.

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