GUDIDData
eudamed_udi Primary ID: 00194545124007

Full Pelvic Assembly, Right Medium (UDI 00194545124007)

Manufactured by Becker Orthopedic Appliance Company

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Full Pelvic Assembly, Right Medium - Primary ID 00194545124007

Device Regulatory Overview

The Full Pelvic Assembly, Right Medium (Model/Catalog Number: 145-RM-1) is a medical device manufactured by Becker Orthopedic Appliance Company. This product is indexed under FDA Product Code / Category Classification Y061215 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
145-RM-1
Product Code / EMDN
Y061215
Device Name
Lerman HARO 2000
Database Sync Date
2026-08-09 16:30:18

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 Full Pelvic Assembly, Right Medium?

The registered manufacturer of record for Full Pelvic Assembly, Right Medium is Becker Orthopedic Appliance Company.

What is the Primary UDI-DI identifier for Full Pelvic Assembly, Right Medium?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00194545124007.

What classification code is assigned to this device?

This device is registered under product classification code Y061215.

Programmatic Export

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

JSON API Endpoint