GUDIDData
gudid Primary ID: EN10112

Polyp Trap with Two Removable Chambers (Non-sterile) (UDI EN10112)

Manufactured by GA Health Company Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Polyp Trap with Two Removable Chambers (Non-sterile) - Primary ID EN10112

Device Regulatory Overview

The Polyp Trap with Two Removable Chambers (Non-sterile) (Model/Catalog Number: EN10112) is a medical device manufactured by GA Health Company Limited. This product is indexed under FDA Product Code / Category Classification CBC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EN10112
Product Code / EMDN
CBC
Device Name
Database Sync Date
2026-08-09 09:46:04

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 Polyp Trap with Two Removable Chambers (Non-sterile)?

The registered manufacturer of record for Polyp Trap with Two Removable Chambers (Non-sterile) is GA Health Company Limited.

What is the Primary UDI-DI identifier for Polyp Trap with Two Removable Chambers (Non-sterile)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EN10112.

What classification code is assigned to this device?

This device is registered under product classification code CBC.

Programmatic Export

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

JSON API Endpoint