gudid Primary ID: Model 4472

Model 4472 (UDI Model 4472)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Model 4472 (Model/Catalog Number: Model 4472) is a medical device manufactured by TUTTNAUER ISRAEL LTD.. This product is indexed under FDA Product Code / Category Classification FLE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Model 4472
Product Code / EMDN: FLE
Device Name: Sterilizer,steam
Database Sync Date: 2026-08-09 09:18:12

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 Model 4472?

The registered manufacturer of record for Model 4472 is TUTTNAUER ISRAEL LTD..

What is the Primary UDI-DI identifier for Model 4472?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Model 4472.

What classification code is assigned to this device?

This device is registered under product classification code FLE.

Similar Classification Devices (FLE)

Other Devices by TUTTNAUER ISRAEL LTD.

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