gudid Primary ID: 15-00170

ESI (UDI 15-00170)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ESI (Model/Catalog Number: 15-00170) is a medical device manufactured by FTT MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification FER within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 15-00170
Product Code / EMDN: FER
Device Name: CCF HIRSCHMAN ANOSCOPE, 5/8" DIAMETER x 2-1/2" LONG WITH ROUNDED OBTURATOR TIP. ACMI FITTING.
Database Sync Date: 2026-08-09 09:34:57

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 ESI?

The registered manufacturer of record for ESI is FTT MEDICAL, INC..

What is the Primary UDI-DI identifier for ESI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15-00170.

What classification code is assigned to this device?

This device is registered under product classification code FER.

Similar Classification Devices (FER)

Other Devices by FTT MEDICAL, INC.

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