gudid Primary ID: DGA-275

Rescue (UDI DGA-275)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Rescue (Model/Catalog Number: DGA-275) is a medical device manufactured by ENDOCHOICE, INC.. This product is indexed under FDA Product Code / Category Classification OCZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DGA-275
Product Code / EMDN: OCZ
Device Name: Alligator Grasping Forceps , Long
Database Sync Date: 2026-08-09 09:31:26

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 Rescue?

The registered manufacturer of record for Rescue is ENDOCHOICE, INC..

What is the Primary UDI-DI identifier for Rescue?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DGA-275.

What classification code is assigned to this device?

This device is registered under product classification code OCZ.

Similar Classification Devices (OCZ)

Other Devices by ENDOCHOICE, INC.

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