classification Primary ID: GCP

Endoscope, Ac-Powered And Accessories (UDI GCP)

Manufactured by

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Endoscope, Ac-Powered And Accessories (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification GCP within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2753-2026 View Full Alert →

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🔒 Compromised Lot & Serial Numbers Locked

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ID: Z-2755-2026 View Full Alert →

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ID: Z-2793-2026 View Full Alert →

SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System...

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Technical Specifications

Model Number: N/A
Product Code / EMDN: GCP
Device Name: Endoscope, Ac-Powered And Accessories
Database Sync Date: 2026-08-09 09:00:27

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 Endoscope, Ac-Powered And Accessories?

The registered manufacturer of record for Endoscope, Ac-Powered And Accessories is .

What is the Primary UDI-DI identifier for Endoscope, Ac-Powered And Accessories?

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

What classification code is assigned to this device?

This device is registered under product classification code GCP.

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