GUDIDData
gudid Primary ID: 5596-1R Model

5596-1R-R-USA (UDI 5596-1R Model)

Manufactured by TUTTNAUER ISRAEL LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 5596-1R-R-USA - Primary ID 5596-1R Model

Device Regulatory Overview

The 5596-1R-R-USA (Model/Catalog Number: 5596-1R Model) 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
5596-1R Model
Product Code / EMDN
FLE
Device Name
Sterilizer,steam
Database Sync Date
2026-08-09 09:18:12

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 5596-1R-R-USA?

The registered manufacturer of record for 5596-1R-R-USA is TUTTNAUER ISRAEL LTD..

What is the Primary UDI-DI identifier for 5596-1R-R-USA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5596-1R Model.

What classification code is assigned to this device?

This device is registered under product classification code FLE.

Programmatic Export

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

JSON API Endpoint