GUDIDData
eudamed_udi Primary ID: 07540194010513

Dr Paley’s Osteotomy System (UDI 07540194010513)

Manufactured by OrthoPediatrics Canada ULC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dr Paley’s Osteotomy System - Primary ID 07540194010513

Device Regulatory Overview

The Dr Paley’s Osteotomy System (Model/Catalog Number: DRPCC-202) is a medical device manufactured by OrthoPediatrics Canada ULC. This product is indexed under FDA Product Code / Category Classification L091103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DRPCC-202
Product Code / EMDN
L091103
Device Name
CLAMP
Database Sync Date
2026-08-09 16:29:06

Full Regulatory Attributes

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{
    "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 Dr Paley’s Osteotomy System?

The registered manufacturer of record for Dr Paley’s Osteotomy System is OrthoPediatrics Canada ULC.

What is the Primary UDI-DI identifier for Dr Paley’s Osteotomy System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07540194010513.

What classification code is assigned to this device?

This device is registered under product classification code L091103.

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