GUDIDData
gudid Primary ID: G36251

NCompass (UDI G36251)

Manufactured by COOK INCORPORATED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NCompass - Primary ID G36251

Device Regulatory Overview

The NCompass (Model/Catalog Number: G36251) is a medical device manufactured by COOK INCORPORATED. This product is indexed under FDA Product Code / Category Classification LQR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
G36251
Product Code / EMDN
LQR
Device Name
NCompass Nitinol Stone Extractor
Database Sync Date
2026-08-09 09:33:19

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 NCompass?

The registered manufacturer of record for NCompass is COOK INCORPORATED.

What is the Primary UDI-DI identifier for NCompass?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G36251.

What classification code is assigned to this device?

This device is registered under product classification code LQR.

Programmatic Export

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

JSON API Endpoint