GUDIDData
eudamed_udi Primary ID: 00841132197028

ORTHOPEDIATRICS® PEDINAIL™ INTRAMEDULLARY NAILING SYSTEM (UDI 00841132197028)

Manufactured by OrthoPediatrics Corp.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ORTHOPEDIATRICS® PEDINAIL™ INTRAMEDULLARY NAILING SYSTEM - Primary ID 00841132197028

Device Regulatory Overview

The ORTHOPEDIATRICS® PEDINAIL™ INTRAMEDULLARY NAILING SYSTEM (Model/Catalog Number: 10-1500-4085-S) is a medical device manufactured by OrthoPediatrics Corp.. This product is indexed under FDA Product Code / Category Classification P09120604 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10-1500-4085-S
Product Code / EMDN
P09120604
Device Name
ORTHOPEDIATRICS® PEDINAIL™ INTRAMEDULLARY NAILING SYSTEM
Database Sync Date
2026-08-09 16:29:17

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 ORTHOPEDIATRICS® PEDINAIL™ INTRAMEDULLARY NAILING SYSTEM?

The registered manufacturer of record for ORTHOPEDIATRICS® PEDINAIL™ INTRAMEDULLARY NAILING SYSTEM is OrthoPediatrics Corp..

What is the Primary UDI-DI identifier for ORTHOPEDIATRICS® PEDINAIL™ INTRAMEDULLARY NAILING SYSTEM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00841132197028.

What classification code is assigned to this device?

This device is registered under product classification code P09120604.

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