GUDIDData
Bulk Audit Tool API Access
gudid Primary ID: 424-9RULER-10

Carriere Motion 3D Ruler (UDI 424-9RULER-10)

Manufactured by Ortho Organizers, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Carriere Motion 3D Ruler - Primary ID 424-9RULER-10

Device Regulatory Overview

The Carriere Motion 3D Ruler (Model/Catalog Number: 424-9RULER-10) is a medical device manufactured by Ortho Organizers, Inc.. This product is indexed under FDA Product Code / Category Classification FTY 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
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
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
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
424-9RULER-10
Product Code / EMDN
FTY
Device Name
Carriere Motion 3D Ruler (10/pack)
Database Sync Date
2026-08-09 09:01:39

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 Carriere Motion 3D Ruler?

The registered manufacturer of record for Carriere Motion 3D Ruler is Ortho Organizers, Inc..

What is the Primary UDI-DI identifier for Carriere Motion 3D Ruler?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 424-9RULER-10.

What classification code is assigned to this device?

This device is registered under product classification code FTY.

Similar Classification Devices (FTY)

Other Devices by Ortho Organizers, Inc.

Programmatic Export

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

JSON API Endpoint